Identity
- Trade Name
- DRYVIEW DVB Laser Imaging Film FDA UDI
- Generic Name
- Medical x-ray film, non-screen FDA UDI
- Device Name
- 100SH 5800 28X35CM (11X14IN) DVB FDA UDI
- Model / Reference
- DRYVIEW DVB Laser Imaging Film FDA UDI
- Description
- 100SH 5800 28X35CM (11X14IN) DVB FDA UDI
Identifiers
- Catalog Number
- 1727817 FDA UDI
- Primary DI / UDI-DI
- 40889971727813 FDA UDI
- FDA Product Code
- IWZ FDA UDI
- GMDN Term
- Medical x-ray film, non-screen FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1840 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
DRYVIEW DVB Laser Imaging Film by Carestream Health, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Carestream Health, Inc.
Sources (1)
- FDA UDI d8fef0a7-e133-4636-a542-cce4f51a3a9d 35 fields · synced Jun 8, 2026