← Back to catalogue

Pomee

FDA UDI

Class I (US FDA UDI)

by Pomee Corporation

Identity

Trade Name
Pomee FDA UDI
Generic Name
Rubber dam clamp FDA UDI
Device Name
RDC #26N Flat jaws for upper molars. FDA UDI
Model / Reference
712-134 FDA UDI
Description
RDC #26N Flat jaws for upper molars. FDA UDI

Identifiers

Catalog Number
712-134 FDA UDI
Primary DI / UDI-DI
G1577121340 FDA UDI
FDA Product Code
EIE FDA UDI
GMDN Term
Rubber dam clamp 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

Yes

FDA UDI

Single Use

No

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: Rubber dam clamp

Pomee by Pomee Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rubber dam clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Pomee Corporation

Sources (1)

  • FDA UDI 53035e8c-fb66-4bdd-9fc9-05a150027828 34 fields · synced Jun 8, 2026