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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 prosthesis/implant abutment screw FDA UDI
Device Name
Clinical Screw for Ti Straumann Bone Level RC 4.1/4.8 FDA UDI
Model / Reference
36018 FDA UDI
Description
Clinical Screw for Ti Straumann Bone Level RC 4.1/4.8 FDA UDI

Identifiers

Catalog Number
36018 FDA UDI
Primary DI / UDI-DI
07332747013856 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental prosthesis/implant abutment screw 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

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

Dimensions & Sizes

Size
Outer Diameter — 4.100 Millimeter FDA UDI

Category: Dental prosthesis/implant abutment screw

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

Similar devices

Also classified as Dental prosthesis/implant abutment screw.

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 43823e5d-2ea1-408d-a64d-dc186aca2cd2 36 fields · synced May 29, 2026