Identity
- Trade Name
- DuLap® FDA UDI
- Generic Name
- Radiopaque woven surgical sponge FDA UDI
- Device Name
- 8 in X 36 in 4 ply Laparotomy Sponges. Washed, Rolled, Loops Tied Wrapped in 2's FDA UDI
- Model / Reference
- 1239VGH FDA UDI
- Description
- 8 in X 36 in 4 ply Laparotomy Sponges. Washed, Rolled, Loops Tied Wrapped in 2's FDA UDI
Identifiers
- Catalog Number
- DUP1239VGH FDA UDI
- Primary DI / UDI-DI
- 00809958016718 FDA UDI
- FDA Product Code
- GDY FDA UDI
- GMDN Term
- Radiopaque woven surgical sponge FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4450 FDA UDI
- Commercial Distribution
- 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
Category: Radiopaque woven surgical sponge
DuLap® by Derma Sciences Canada, Inc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Derma Sciences Canada, Inc
Sources (1)
- FDA UDI 002f9cf6-1f63-4eb5-a55c-46c310671644 36 fields · synced May 30, 2026