Identity
- Trade Name
- Steri-Drape™ FDA UDI
- Generic Name
- Patient surgical drape, single-use FDA UDI
- Device Name
- 3M™ Steri-Drape™ X-ray Cassette Drape 1008 FDA UDI
- Model / Reference
- 1008 FDA UDI
- Description
- 3M™ Steri-Drape™ X-ray Cassette Drape 1008 FDA UDI
Identifiers
- Catalog Number
- 1008 FDA UDI
- Primary DI / UDI-DI
- 50707387222371 FDA UDI
- FDA Product Code
- PUI FDA UDI
- GMDN Term
- Patient surgical drape, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4370 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Steri-Drape™ by 3m Company — 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
- 3m Company
Sources (1)
- FDA UDI 8ff28f02-b310-405c-95b2-b906d1907cdd 36 fields · synced May 30, 2026