№ lp_1_2_46037
File format: docx Character count: 6633 File size: 49 KB
The document provides technical specifications for the FaceStation F2, a biometric access control device, detailing its features, installation guidelines, and compliance with international standards.
Year: 2023
Region / City: Republic of Korea
Topic: Biometric Access Control System
Document Type: Technical Specifications
Organization / Institution: Suprema Inc.
Author: Suprema Inc.
Target Audience: System integrators, installers, and IT professionals
Period of validity: Not specified
Approval Date: Not specified
Amendment Date: Not specified
Price: 8 / 10 USD
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SUPREMA OUTDOOR COMPACT RFID DEVICE – XPass 2 TECHNICAL SPECIFICATIONS
Year: 2025
Region / City: Seongnam-si, Gyeonggi-do, Republic of Korea
Subject: RFID device specifications
Document type: Technical Specification
Organization / Institution: Suprema Inc.
Author: Suprema Inc.
Target audience: Technicians, engineers, and system integrators in access control systems
Effective period: Indefinite
Approval date: 2025-07-23
Modification date: Not specified
Medical and Research Device Risk Assessment Vendor Packet Instructions
Year: 2020
Region / City: Rochester, MN
Topic: Cybersecurity of medical and research devices
Document type: Vendor packet
Organization / Institution: Mayo Clinic
Author: Mayo Clinic
Target audience: Vendors, healthcare technology management teams
Period of validity: N/A
Approval date: N/A
Date of amendments: N/A
Annex 1 to Guidance on filling in the JCA dossier template of a Medical Device - Table template collection V1.028 NOVEMBER 2025
Year: 2025
Region / city: EU
Topic: Health Technology Assessment
Document Type: Guidance
Organization / Institution: HTA CG
Author: European Commission
Target audience: Professionals in Health Technology Assessment
Validity period: From 28 NOVEMBER 2025
Approval date: 28 NOVEMBER 2025
Amendment date: Not specified
IoT Device Connection Efficiency Test Book Version 7.116 September 2023
Year: 2023
Region / City: Global
Topic: Internet of Things, IoT Device Testing
Document Type: Industry Specification
Organization / Institution: GSMA
Author: GSMA
Target Audience: Mobile Network Operators, IoT Service Providers, IoT Device Makers, IoT Device Application Developers, Communication Module Vendors, Radio Baseband Chipset Vendors
Validity Period: N/A
Approval Date: N/A
Amendment Date: N/A
Description: Industry specification document outlining test cases for IoT device compliance with GSMA IoT Device Connection Efficiency Guidelines, focusing on device behavior and network resource management.
Request for Quotation for Quality Management System Certification and if applicable Conformity Assessment Activities for Medical Device Regulation
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Continuing review of non-research Humanitarian Use Device (HUD) using the expedited procedure
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IoT Device Connection Efficiency Guidelines Version 12.005 May 2025
Year: 2025
Region / city: Global
Topic: Internet of Things (IoT)
Document Type: Industry Specification
Organization / Institution: GSM Association
Author: GSM Association
Target audience: Mobile Network Operators, IoT Device Manufacturers, IoT Device Application Developers
Period of validity: Ongoing
Approval date: May 2025
Date of changes: Not specified
Service specification: NHS lateral flow device tests supply service for patients potentially eligible for COVID-19 treatments Advanced service Version 4: May 2025 (updated 01 May 2025)
Year: 2025
Region / City: United Kingdom
Topic: COVID-19 treatment, lateral flow device tests
Document Type: Service Specification
Organization / Institution: NHS England
Author: NHS England
Target Audience: Pharmacy contractors, healthcare professionals
Period of Validity: Ongoing, from 6 November 2023
Date of Approval: May 2025
Date of Changes: 01 May 2025
Informed Consent for Emergency Use/Treatment with an Unapproved Drug / Biologic / Device 16.315 (HRP-506)
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Subject: Emergency Use Treatment
Document Type: Informed Consent Form
HDA Standard Pharmaceutical (Rx-only) Product and Medical Device Information Short Form Instructions
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Theme: Pharmaceutical products, Medical devices
Document type: Instructions, Form
Organization / Institution: HDA
Target audience: Distributors, Manufacturers, Supply chain professionals
Periodic Safety Update Report for [Device Name]
Year: XXXX
Region / City: XXX
Theme: Post-market Surveillance
Document Type: Report
Organization: XXX
Author: XXX
Target Audience: Regulatory Authorities, Healthcare Professionals
Period of Validity: [start date] - [end date]
Approval Date: YYYY-MM-DD
Revision Date: YYYY-MM-DD
Post-Market Clinical Follow-Up (PMCF) Plan for [Device Name]
Year: YYYY
Region / City: [City/Region]
Topic: Medical Device Safety and Performance Monitoring
Document Type: PMCF Plan
Organization: [Manufacturer Name]
Author: [Author Name]
Target Audience: Regulatory Authorities, Medical Device Manufacturers
Validity Period: YYYY/MM/DD to YYYY/MM/DD
Approval Date: DD/MM/YYYY
Revision Date: XXXX
Date of Changes: YYYY/MM/DD
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Year: 2020
Region / city: Not specified
Theme: Defense, Technology Development
Document Type: Statement of Objectives
Organization / Institution: Not specified
Author: Not specified
Target Audience: Defense contractors, technology developers
Period of validity: Not specified
Approval date: Not specified
Modification date: Not specified
Intra-uterine device (IUD) insertion information and consent form
Note: Year
Subject: Contraception, Medical Procedure
Document Type: Patient Information and Consent Form
Target Audience: Patients, Healthcare Providers
Investigational Device Accountability Log – Site (EU MDR, 2021)
Document type: Accountability log
Scope: Clinical investigation site
Subject matter: Investigational medical devices
Regulatory framework: EU Regulation 2017/745 on Medical Devices (MDR)
Applicable date: 26 May 2021
Version date: 18 August 2021
Responsible organization: Kliniska Studier Sverige
Responsible network: National network for clinical investigations with medical devices within Clinical Studies Sweden
Geographical context: Sweden
Intended setting: Clinical investigation site(s)
Signatory role: Principal Investigator
Source category: Clinical research documentation
HDA Standard Pharmaceutical (Rx-only) Product and Medical Device Information Form Instructions
Year: 2021
Region / City: United States
Topic: Pharmaceutical and Medical Device Product Information
Document Type: Instructional Form
Organization / Institution: Health Distribution Alliance (HDA)
Author: Health Distribution Alliance
Target Audience: Pharmaceutical distributors, medical device manufacturers, suppliers
Effective Period: Not specified
Approval Date: Not specified
Amendment Date: 2021
Topics: FaceStation SUPREMA Device