← Back to catalogue

Hedy Dental Dam

FDA UDI

Class I (US FDA UDI)

by AMD Medicom Inc

Identity

Trade Name
HEDY DENTAL DAM FDA UDI
Generic Name
Rubber dam, non-latex FDA UDI
Device Name
HEDY Polyisoprene Dental Dam - Non-Latex - 6" x 6" - Heavy - Blue FDA UDI
Model / Reference
320DNB-6H FDA UDI
Description
HEDY Polyisoprene Dental Dam - Non-Latex - 6" x 6" - Heavy - Blue FDA UDI

Identifiers

Catalog Number
320DNB-6H FDA UDI
Primary DI / UDI-DI
10686864060434 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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, non-latex

Hedy Dental Dam by AMD Medicom Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rubber dam, non-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

Manufacturer
AMD Medicom Inc

Sources (1)

  • FDA UDI 2cae057f-7d85-4aba-8a5b-28e4c7b3eb2a 36 fields · synced Jun 6, 2026