Identity
- Trade Name
- Medi-First Latex Medium Finger Cots FDA UDI
- Generic Name
- Surgical/examination garment kit FDA UDI
- Device Name
- A non-powdered patient disposable latex 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
- 70435 FDA UDI
- Description
- A non-powdered patient disposable latex 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
- 70435 FDA UDI
- Primary DI / UDI-DI
- 00347682704353 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 Latex Medium Finger Cots 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 f0467d61-b007-4aad-a442-231d812da1de 35 fields · synced Jun 8, 2026