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Staydent

FDA UDI

Class I (US FDA UDI)

by Sheffield Pharmaceuticals LLC

Identity

Trade Name
Staydent FDA UDI
Generic Name
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free FDA UDI
Device Name
Denture Adhesive Cream FDA UDI
Model / Reference
NS 5501C FDA UDI
Description
Denture Adhesive Cream FDA UDI

Identifiers

Catalog Number
17024024 FDA UDI
Primary DI / UDI-DI
00732953170249 FDA UDI
FDA Product Code
KOO FDA UDI
GMDN Term
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3490 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

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: Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free

Staydent by Sheffield Pharmaceuticals LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sheffield Pharmaceuticals LLC

Sources (1)

  • FDA UDI 602ccbd2-c8cb-4eac-adc7-d445a07afd14 35 fields · synced May 30, 2026