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PremierPro

FDA UDI

Class I (US FDA UDI)

by Svs Llc

Identity

Trade Name
PremierPro FDA UDI
Generic Name
Non-adhesive device retention bandage FDA UDI
Device Name
Cohesive Bandage, Non-Sterile, 4" x 5" Stretched, Tan, Not made with Natural Rubber Latex FDA UDI
Model / Reference
8944 FDA UDI
Description
Cohesive Bandage, Non-Sterile, 4" x 5" Stretched, Tan, Not made with Natural Rubber Latex FDA UDI

Identifiers

Catalog Number
8944 FDA UDI
Primary DI / UDI-DI
00818566016706 FDA UDI
FDA Product Code
FQM FDA UDI
KGX FDA UDI
GMDN Term
Non-adhesive device retention bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
880.5240 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-adhesive device retention bandage

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

Similar devices

Also classified as Non-adhesive device retention bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Svs Llc

Sources (1)

  • FDA UDI a5ae9f3d-ebe1-47ab-a179-6aaf9ac1e9a3 36 fields · synced Jun 8, 2026