Identity
- Trade Name
- Medi-First Large Latex Finger Cot FDA UDI
- Generic Name
- Surgical/examination garment kit FDA UDI
- Device Name
- A non-powdered latex patient examination disposable device intended for medical purposes that is worn on the examiner's finger to prevent contamination between patient and examiner (144 count). FDA UDI
- Model / Reference
- 72235 FDA UDI
- Description
- A non-powdered latex patient examination disposable device intended for medical purposes that is worn on the examiner's finger to prevent contamination between patient and examiner (144 count). FDA UDI
Identifiers
- Catalog Number
- 72235 FDA UDI
- Primary DI / UDI-DI
- 00347682722357 FDA UDI
- FDA Product Code
- LZB FDA UDI
- GMDN Term
- Surgical/examination garment kit 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
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical/examination garment kit
Medi-First Large Latex Finger Cot by Medique Products — 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
- Medique Products
Sources (1)
- FDA UDI 68287f3f-ae52-4271-b662-9b6f3a7172d4 35 fields · synced May 30, 2026