← Back to catalogue

Dentech

FDA UDI

Class I (US FDA UDI)

by Dentech Corp.

Identity

Trade Name
DENTECH FDA UDI
Generic Name
Rubber dam clamp FDA UDI
Model / Reference
01014917 FDA UDI

Identifiers

Primary DI / UDI-DI
04560218669568 FDA UDI
FDA Product Code
EEF 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

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rubber dam clamp

Dentech by Dentech Corp. — 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
Dentech Corp.

Sources (1)

  • FDA UDI 4b8c6da4-add2-46b2-ba61-bdb3fe219be2 32 fields · synced Jun 1, 2026