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NobelProcera®

FDA UDI

Class II (US FDA UDI)

by Nobel Biocare AG

Identity

Trade Name
NobelProcera® FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
NobelProcera Imp Br Zr Ab Lev 7u Medium FDA UDI
Model / Reference
71406 FDA UDI
Description
NobelProcera Imp Br Zr Ab Lev 7u Medium FDA UDI

Identifiers

Catalog Number
71406 FDA UDI
Primary DI / UDI-DI
07332747120011 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, permanent, preformed

NobelProcera® by Nobel Biocare AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Manufacturer
Nobel Biocare AG

Sources (1)

  • FDA UDI 400b188e-879a-4fea-91f2-153f704bbd8f 36 fields · synced May 31, 2026