Identity
- Trade Name
- Sugi FDA UDI
- Generic Name
- Surgical scrub sponge FDA UDI
- Device Name
- Sugi Instrument Wipe Xtra, non-sterile, 80 x 80 mm, 250 pcs. FDA UDI
- Model / Reference
- 31963 FDA UDI
- Description
- Sugi Instrument Wipe Xtra, non-sterile, 80 x 80 mm, 250 pcs. FDA UDI
Identifiers
- Catalog Number
- 31963 FDA UDI
- Primary DI / UDI-DI
- 04260306710508 FDA UDI
- FDA Product Code
- FEB FDA UDI
- GMDN Term
- Surgical scrub sponge FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Sugi by QuestAlpha GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- QuestAlpha GmbH & Co. KG
Sources (1)
- FDA UDI 97d570f4-755a-4096-a914-d937e456e2a8 35 fields · synced May 31, 2026