Identity
- Trade Name
- Ultracell® FDA UDI
- Generic Name
- Medical device cleaning sponge/set FDA UDI
- Device Name
- 'INSTRUMENT WIPE, FOIL POUCHED 3'' X 3'' X 2MM (300/SP)' FDA UDI
- Model / Reference
- S90900 FDA UDI
- Description
- 'INSTRUMENT WIPE, FOIL POUCHED 3'' X 3'' X 2MM (300/SP)' FDA UDI
Identifiers
- Catalog Number
- S90900 FDA UDI
- Primary DI / UDI-DI
- 30886158012086 FDA UDI
- FDA Product Code
- HOZ FDA UDI
- GMDN Term
- Medical device cleaning sponge/set FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.4790 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
No
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
Radiation Sterilization FDA UDI
Category: Medical device cleaning sponge/set
Ultracell® by Beaver-Visitec International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- First Step Bedside Kit - Stand-Up Pouch, Gemini Cleaning Pad — CYGNUS MEDICAL L.L.C. · Class I
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- MEDLINE — MEDLINE INDUSTRIES, INC. · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Beaver-Visitec International, Inc.
Sources (1)
- FDA UDI 551c4fbc-f7ca-43ca-92dd-85ba639267c3 36 fields · synced Jun 8, 2026