← Back to catalogue

Unit Expanded, Castable For Esthetic Abutment, Universal Platform

FDA UDI

Class I (US FDA UDI)

by Biotechnology Institute Sl

Identity

Trade Name
UNIT EXPANDED, CASTABLE FOR ESTHETIC ABUTMENT, UNIVERSAL PLATFORM FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Model / Reference
CPTZMIUPUEX FDA UDI

Identifiers

Primary DI / UDI-DI
08435389819035 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use 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

Yes

FDA UDI

Implantable

Yes

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

Category: Dental implant suprastructure, temporary, preformed, single-use

Unit Expanded, Castable For Esthetic Abutment, Universal Platform by Biotechnology Institute Sl — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

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

Sources (1)

  • FDA UDI 7f1a7c41-853c-4ba0-9f94-4c6c3e8e23c7 32 fields · synced May 31, 2026