Identity
- Trade Name
- 3M™ Steri-Drape™ FDA UDI
- Generic Name
- Patient surgical drape, single-use FDA UDI
- Device Name
- 3M™ Steri-Drape™ Incise Drape, 1035, Incise Area 10 cm x 20 cm (3 7/8 in x 7 7/8 in), 10/Carton, 4 Cartons/Case FDA UDI
- Model / Reference
- 1035 FDA UDI
- Description
- 3M™ Steri-Drape™ Incise Drape, 1035, Incise Area 10 cm x 20 cm (3 7/8 in x 7 7/8 in), 10/Carton, 4 Cartons/Case FDA UDI
Identifiers
- Catalog Number
- 1035 FDA UDI
- Primary DI / UDI-DI
- 30707387793013 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
- 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
Yes
FDA UDI
Category: Patient surgical drape, single-use
3M™ Steri-Drape™ by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- 3m Company
Sources (1)
- FDA UDI 0ade74f1-cc9b-46bb-9884-6a2d06505a0a 35 fields · synced Jun 8, 2026