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Artman Instruments

FDA UDI

Class I (US FDA UDI)

by Wise Linkers Llc

Identity

Trade Name
Artman Instruments FDA UDI
Generic Name
Rubber dam clamp FDA UDI
Device Name
Rubber Dam Clamps Organizer Rack for 12 pcs ARTMAN FDA UDI
Model / Reference
7E3RGX1YBO FDA UDI
Description
Rubber Dam Clamps Organizer Rack for 12 pcs ARTMAN FDA UDI

Identifiers

Catalog Number
1 FDA UDI
Primary DI / UDI-DI
D1277E3RGX1YBO1 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rubber dam clamp

Artman Instruments by Wise Linkers Llc — 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

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Manufacturer

Manufacturer
Wise Linkers Llc

Sources (1)

  • FDA UDI eb76d87b-b798-4ed3-85dd-19c7ead573cc 34 fields · synced May 30, 2026