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PremierPro

FDA UDI

Class I (US FDA UDI)

by Svs Llc

Identity

Trade Name
PremierPro FDA UDI
Generic Name
Absorbent underpad, non-antimicrobial, single-use FDA UDI
Device Name
Underpad, Plus Fluff, Heavy Absorbency, 36" x 36", 12/bg FDA UDI
Model / Reference
6609PP FDA UDI
Description
Underpad, Plus Fluff, Heavy Absorbency, 36" x 36", 12/bg FDA UDI

Identifiers

Catalog Number
6609PP FDA UDI
Primary DI / UDI-DI
00818566017970 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Absorbent underpad, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6060 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: Absorbent underpad, non-antimicrobial, single-use

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

Similar devices

Also classified as Absorbent underpad, non-antimicrobial, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Svs Llc

Sources (1)

  • FDA UDI c1f3dfe6-9cca-491a-b63f-ccbaa9117a86 35 fields · synced Jun 8, 2026