Identity
- Trade Name
- Vita Flex CR System FDA UDI
- Generic Name
- Computed radiography digital imaging scanner FDA UDI
- Device Name
- NB Vita Flex CR 30PPH solution PC/Monito FDA UDI
- Model / Reference
- Vita Flex CR System FDA UDI
- Description
- NB Vita Flex CR 30PPH solution PC/Monito FDA UDI
Identifiers
- Catalog Number
- 1069400 FDA UDI
- Primary DI / UDI-DI
- 60889971069405 FDA UDI
- FDA Product Code
- MQB FDA UDI
- GMDN Term
- Computed radiography digital imaging scanner FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1680 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Vita Flex CR System by Carestream Health, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Carestream Health, Inc.
Sources (1)
- FDA UDI 26e84b63-867e-4e5a-878f-d6a63290904a 35 fields · synced Jun 8, 2026