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DG Health

FDA UDI

Class I (US FDA UDI)

by Dolgencorp, Llc

Identity

Trade Name
DG Health FDA UDI
Generic Name
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free FDA UDI
Device Name
Denture Adhesive, Original FDA UDI
Model / Reference
QWC FDA UDI
Description
Denture Adhesive, Original FDA UDI

Identifiers

Primary DI / UDI-DI
00071031938532 FDA UDI
FDA Product Code
KOT 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
Not 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

DG Health by Dolgencorp, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dolgencorp, Llc

Sources (1)

  • FDA UDI 698fbed9-4b56-4015-8084-c140c53c3d46 34 fields · synced May 30, 2026