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MiniDam

FDA UDI

Class I (US FDA UDI)

by DMG Chemisch-Pharmazeutische Fabrik GmbH

Identity

Trade Name
MiniDam FDA UDI
Generic Name
Rubber dam, non-latex FDA UDI
Device Name
Gingival guard, silicone. Content: 20 Pieces FDA UDI
Model / Reference
220381 FDA UDI
Description
Gingival guard, silicone. Content: 20 Pieces FDA UDI

Identifiers

Catalog Number
220381 FDA UDI
Primary DI / UDI-DI
EDMG2203811 FDA UDI
FDA Product Code
EIE FDA UDI
GMDN Term
Rubber dam, non-latex FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6300 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

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rubber dam, non-latex

A comprehensive medical device directory listing the MiniDam, a dental rubber dam used to isolate and protect the patient during procedures. It is designed for single-use and non-latex allergy patients.

Similar devices

Also classified as Rubber dam, non-latex.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a0fb6f4c-dac9-42b7-b9ce-49ccb9274155 36 fields · synced Aug 3, 2026