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EdgeDam™ Refill Medium 5x5 Latex-Free

FDA UDI

Class I (US FDA UDI)

by Clinician's Choice Dental Products, Inc.

Identity

Trade Name
EdgeDam™ Refill Medium 5x5 Latex-Free FDA UDI
Generic Name
Rubber dam, non-latex FDA UDI
Device Name
Premium Polyisoprene Dental Dam FDA UDI
Model / Reference
EDVLFM5550 FDA UDI
Description
Premium Polyisoprene Dental Dam FDA UDI

Identifiers

Catalog Number
EDVLFM5550 FDA UDI
Primary DI / UDI-DI
07540172019422 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

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

No

FDA UDI

Dimensions & Sizes

Size
Area/Surface Area — 25 Square inch FDA UDI

Category: Rubber dam, non-latex

EdgeDam™ Refill Medium 5x5 Latex-Free by Clinician's Choice Dental Products, 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

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Manufacturer

Sources (1)

  • FDA UDI ea36ee8b-441a-48c3-8889-4869625420cf 37 fields · synced Jun 7, 2026