← Back to catalogue

PremierPro

FDA UDI

Class I (US FDA UDI)

by Svs Llc

Identity

Trade Name
PremierPro FDA UDI
Generic Name
Vinyl examination/treatment glove, non-powdered FDA UDI
Device Name
PremierPro Powder Free Vinyl Exam Glove Standard Large 100 count FDA UDI
Model / Reference
4044 FDA UDI
Description
PremierPro Powder Free Vinyl Exam Glove Standard Large 100 count FDA UDI

Identifiers

Catalog Number
4044 FDA UDI
Primary DI / UDI-DI
00854344002523 FDA UDI
510(k) Number
K100326 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

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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: Vinyl examination/treatment glove, non-powdered

PremierPro by Svs Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Svs Llc

Sources (1)

  • FDA UDI c372bba9-f0e9-4fb1-b4f6-b28ca3c6ab10 36 fields · synced Jun 8, 2026