Identity
- Trade Name
- MEDLINE FDA UDI
- Generic Name
- Radiopaque woven surgical sponge FDA UDI
- Device Name
- SPONGE,STICK,1-1/4 L,XR,5/PK,NS,500/CS FDA UDI
- Model / Reference
- BNS44013 FDA UDI
- Description
- SPONGE,STICK,1-1/4 L,XR,5/PK,NS,500/CS FDA UDI
Identifiers
- Catalog Number
- BNS44013 FDA UDI
- Primary DI / UDI-DI
- 30193489088810 FDA UDI
- FDA Product Code
- NAB FDA UDI
- GMDN Term
- Radiopaque woven surgical sponge FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4014 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
Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Radiopaque woven surgical sponge.
- SurgiCount Safety-Sponge — Stryker Corp. · Class I
- DuLap® — Derma Sciences Canada, Inc · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- ORLocate — STERIS CORPORATION · Class I
- Kerlix — Cardinalhealth · Class I
- AMD-RITMED — AMD Medicom Inc · Class I
- Dukal — Dukal LLC · Class I
- HCS — DYAD MEDICAL SOURCING, LLC · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medline Industries, Inc.
Sources (1)
- FDA UDI 03e742c8-9350-46f6-ab9e-7a9681a83de7 35 fields · synced Jun 8, 2026