← Back to catalogue

Ultradent

FDA UDI

Class I (US FDA UDI)

by Four D Rubber Company Limited

Identity

Trade Name
Ultradent FDA UDI
Generic Name
Rubber dam, Hevea-latex FDA UDI
Device Name
DermaDam Latex Medium - 52pk FDA UDI
Model / Reference
Medium FDA UDI
Description
DermaDam Latex Medium - 52pk FDA UDI

Identifiers

Catalog Number
DENTALAUPIBLU01800552 FDA UDI
Primary DI / UDI-DI
05060748681997 FDA UDI
FDA Product Code
EIE FDA UDI
GMDN Term
Rubber dam, Hevea-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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Rubber dam, Hevea-latex

Ultradent by Four D Rubber Company Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rubber dam, Hevea-latex.

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

Sources (1)

  • FDA UDI 116dba2d-2e7d-45aa-a045-ba2b528440c4 35 fields · synced May 30, 2026