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NobelReplace®

FDA UDI

Class I (US FDA UDI)

by Nobel Biocare AG

Identity

Trade Name
NobelReplace® FDA UDI
Generic Name
Bone tap, single-use FDA UDI
Device Name
Screw Tap NobRpl 6.0/Bmk Syst WP Ø6 7-13mm FDA UDI
Model / Reference
32294 FDA UDI
Description
Screw Tap NobRpl 6.0/Bmk Syst WP Ø6 7-13mm FDA UDI

Identifiers

Catalog Number
32294 FDA UDI
Primary DI / UDI-DI
07332747008722 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Bone tap, 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

Dimensions & Sizes

Size
Outer Diameter — 6.000 Millimeter FDA UDI

Category: Bone tap, single-use

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

Similar devices

Also classified as Bone tap, single-use.

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 f9a8581c-08d2-4105-95e2-7d277cf9a451 36 fields · synced May 30, 2026