Identity
- Trade Name
- A Plus FDA UDI
- Generic Name
- Radiopaque woven surgical sponge FDA UDI
- Device Name
- Bulk Lap Sponges , 17"X26", X-Ray Detectable, Prewashed, Steam Pretreatment, White, No Optical Brightener , 5 Pc(s)/Bundle, 500 Pc(s)/Case FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- Bulk Lap Sponges , 17"X26", X-Ray Detectable, Prewashed, Steam Pretreatment, White, No Optical Brightener , 5 Pc(s)/Bundle, 500 Pc(s)/Case FDA UDI
Identifiers
- Catalog Number
- LS-1726-PS FDA UDI
- Primary DI / UDI-DI
- 00683534840115 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Radiopaque woven surgical sponge
A Plus by A Plus International, 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
- A Plus International, Inc
Sources (1)
- FDA UDI 3696331b-cf83-4e07-ab66-a98879db4bd7 34 fields · synced Jun 1, 2026