NobelActive®

FDA UDI

Class I (US FDA UDI)

by Nobel Biocare AG

Identity

Trade Name: NobelActive® FDA UDI
Generic Name: Bone tap, single-use FDA UDI
Device Name: Guided Screw Tap NobelActive® RP 5.0x8.5-10mm FDA UDI
Model / Reference: 35880 FDA UDI
Description: Guided Screw Tap NobelActive® RP 5.0x8.5-10mm FDA UDI

Identifiers

Catalog Number: 35880 FDA UDI
Primary DI / UDI-DI: 07332747015591 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 10.000 Millimeter FDA UDI
Outer Diameter — 5.000 Millimeter FDA UDI

Category: Bone tap, single-use

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Nobel Biocare AG

Sources (1)

FDA UDI c1e7da72-210c-434b-aa1f-2fa15b971edf 36 fields · synced May 30, 2026