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Imetric

FDA UDI

Class I (US FDA UDI)

by Imetric 4D Imaging Sarl

Identity

Trade Name
Imetric FDA UDI
Generic Name
Dental implant abutment analog, intraoral-scanning, reusable FDA UDI
Device Name
ICamBody C: IMP TRI® - Matrix® - P37 (01-08) FDA UDI
Model / Reference
ICB-TRMA-37-01-08 FDA UDI
Description
ICamBody C: IMP TRI® - Matrix® - P37 (01-08) FDA UDI

Identifiers

Catalog Number
ICB-TRMA-37-01-08 FDA UDI
Primary DI / UDI-DI
07640243230272 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant abutment analog, intraoral-scanning, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant abutment analog, intraoral-scanning, reusable

Imetric by Imetric 4D Imaging Sarl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant abutment analog, intraoral-scanning, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Imetric 4D Imaging Sarl

Sources (1)

  • FDA UDI 9668be9b-0df1-4baf-a453-5a4a64e791aa 35 fields · synced May 30, 2026