Identity
- Trade Name
- QG-TV-IP-FM FDA UDI
- Generic Name
- X-ray system computer, diagnostic, general-purpose FDA UDI
- Device Name
- QG-TV10-IPF-MAT TECHVISION QS-550 DRX AT FDA UDI
- Model / Reference
- QG-TV-IP-FM FDA UDI
- Description
- QG-TV10-IPF-MAT TECHVISION QS-550 DRX AT FDA UDI
Identifiers
- Catalog Number
- 6573349 FDA UDI
- Primary DI / UDI-DI
- 60889976573341 FDA UDI
- FDA Product Code
- LMD FDA UDIIZO FDA UDI
- GMDN Term
- X-ray system computer, diagnostic, general-purpose FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.2020 FDA UDI892.1700 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: X-ray system computer, diagnostic, general-purpose
Qg-Tv-Ip-Fm by Carestream Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as X-ray system computer, diagnostic, general-purpose.
- InfiMed Digital Imaging System, Precision MPi, RF, CCD Camera — Varex Imaging Corporation · Class II
- Varex Digital Imaging System, Nexus, DRF, v3.1.0 — Varex Imaging Corporation · Class II
- Varex Digital Imaging Software, Nexus DR, v4.12 — Varex Imaging Corporation · Class II
- Varex Digital Imaging Software, Nexus DR, v4.13 — Varex Imaging Corporation · Class II
- Varex Digital Imaging System, Nexus DR v4.1.0 — Varex Imaging Corporation · Class II
- InfiMed Digital Imaging System, Precision RXi, RF/DSA, CCD Camera — Varex Imaging Corporation · Class II
- InfiMed Digital Imaging System, Platinum One, DSA, CCD Camera — Varex Imaging Corporation · Class II
- Varex Digital Imaging Software, Nexus, DR, v3.2 — Varex Imaging Corporation · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Carestream Health, Inc.
Sources (1)
- FDA UDI 40734614-6fe7-4ccf-aa23-871c9cfc3cfd 34 fields · synced Jun 8, 2026