Identity
- Trade Name
- AdvanceFit FDA UDI
- Generic Name
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
- Device Name
- 4.5mil, 9.5" in Length, Nitrile, Examination Grade, Ambidextrous, Powder Free, Beaded Cuff, Black Color, Size 2X-Large Sample Pack FDA UDI
- Model / Reference
- 650-BK-2XL FDA UDI
- Description
- 4.5mil, 9.5" in Length, Nitrile, Examination Grade, Ambidextrous, Powder Free, Beaded Cuff, Black Color, Size 2X-Large Sample Pack FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850019992380 FDA UDI
- FDA Product Code
- LZA FDA UDI
- GMDN Term
- Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6250 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Nitrile examination/treatment glove, non-powdered, non-antimicrobial
AdvanceFit by Summit Glove 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
- Summit Glove Inc.
Sources (1)
- FDA UDI 6c43d1c2-ba9c-49cb-991a-50abef3b04e0 34 fields · synced Jun 6, 2026