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Gold Cylinder For Multi-Im® Abutment, Tiny®, Narrow & Universal Platforms

FDA UDI

Class II (US FDA UDI)

by Biotechnology Institute Sl

Identity

Trade Name
GOLD CYLINDER FOR MULTI-IM® ABUTMENT, TINY®, NARROW & UNIVERSAL PLATFORMS FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Model / Reference
COMIPEU FDA UDI

Identifiers

Primary DI / UDI-DI
08435389803706 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Gold Cylinder For Multi-Im® Abutment, Tiny®, Narrow & Universal Platforms by Biotechnology Institute Sl — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b2cd6b1f-9e41-4279-9165-16fe6b96a98c 33 fields · synced May 31, 2026