← Back to catalogue

Nobel Biocare®

FDA UDI

Class I (US FDA UDI)

by Nobel Biocare AG

Identity

Trade Name
Nobel Biocare® FDA UDI
Generic Name
Screw extractor, single-use FDA UDI
Device Name
Screw Tap Repair M2.0 FDA UDI
Model / Reference
37517 FDA UDI
Description
Screw Tap Repair M2.0 FDA UDI

Identifiers

Catalog Number
37517 FDA UDI
Primary DI / UDI-DI
07332747084283 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Screw extractor, 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Screw extractor, single-use

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

Similar devices

Also classified as Screw extractor, 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

Manufacturer
Nobel Biocare AG

Sources (1)

  • FDA UDI 7bb0357d-fb1d-47fd-979a-a0dc9e2e46f4 35 fields · synced May 31, 2026