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Platinum

FDA UDI

Class I (US FDA UDI)

by M.Y.T. USA Corp.

Identity

Trade Name
PLATINUM FDA UDI
Generic Name
Vinyl examination/treatment glove, non-powdered FDA UDI
Device Name
VINYL EXAM GLOVES FDA UDI
Model / Reference
VINYL EXAM GLOVES SIZE MEDIUM FDA UDI
Description
VINYL EXAM GLOVES FDA UDI

Identifiers

Primary DI / UDI-DI
00840169153601 FDA UDI
FDA Product Code
LYZ FDA UDI
GMDN Term
Vinyl 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vinyl examination/treatment glove, non-powdered

Platinum by M.Y.T. USA Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vinyl examination/treatment glove, non-powdered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
M.Y.T. USA Corp.

Sources (1)

  • FDA UDI 8758e0e6-8904-41ae-8c40-52d231f4cfa1 33 fields · synced May 29, 2026