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Biodam

FDA UDI

Class I (US FDA UDI)

by Four D Rubber Company Limited

Identity

Trade Name
BIODAM FDA UDI
Generic Name
Rubber dam, Hevea-latex FDA UDI
Device Name
BIODAM Sample Blue Latex Dam - Thin 6" - 1pc FDA UDI
Model / Reference
Thin FDA UDI
Description
BIODAM Sample Blue Latex Dam - Thin 6" - 1pc FDA UDI

Identifiers

Catalog Number
SAMPLLABIOBLU01500601 FDA UDI
Primary DI / UDI-DI
05060748681829 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

Biodam 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

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Manufacturer

Sources (1)

  • FDA UDI 96dd5103-28fb-4ad9-a07b-86f5e87ed18d 35 fields · synced Jun 6, 2026