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Externa® Wide Implant Impression Coping - Indirect Technique Rotating Ø 5, 5mm L

FDA UDI

Class I (US FDA UDI)

by Biotechnology Institute Sl

Identity

Trade Name
EXTERNA® WIDE IMPLANT IMPRESSION COPING - INDIRECT TECHNIQUE ROTATING Ø 5,5MM L FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, reusable FDA UDI
Model / Reference
CIRIA5 FDA UDI

Identifiers

Primary DI / UDI-DI
08435389824855 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, temporary, preformed, reusable

Externa® Wide Implant Impression Coping - Indirect Technique Rotating Ø 5, 5mm L by Biotechnology Institute Sl — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biotechnology Institute Sl

Sources (1)

  • FDA UDI d22ae754-0a93-466d-9071-60b0a1fa2cb1 32 fields · synced Jun 8, 2026