Identity
- Trade Name
- Next Generation Stretch Vinyl Exam Gloves FDA UDI
- Generic Name
- Ethylene vinyl acetate examination/treatment glove, non-powdered FDA UDI
- Device Name
- Next Generation Stretch Vinyl Exam Gloves, Powder-Free, Small FDA UDI
- Model / Reference
- 6822 FDA UDI
- Description
- Next Generation Stretch Vinyl Exam Gloves, Powder-Free, Small FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00709553682229 FDA UDI
- 510(k) Number
- K100486 FDA UDI
- FDA Product Code
- LYZ FDA UDI
- GMDN Term
- Ethylene vinyl acetate examination/treatment glove, non-powdered 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Category: Ethylene vinyl acetate examination/treatment glove, non-powdered
Next Generation Stretch Vinyl Exam Gloves by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Dynarex Corp.
Sources (1)
- FDA UDI 05365bd6-7f2d-47b0-8755-4fc696210e8a 34 fields · synced Jun 8, 2026