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Nobel Biocare®

FDA UDI

Class I (US FDA UDI)

by Nobel Biocare AG

Identity

Trade Name
Nobel Biocare® FDA UDI
Generic Name
Dental soft-tissue coring punch, reusable FDA UDI
Device Name
Tissue Punch 3.0 FDA UDI
Model / Reference
28910 FDA UDI
Description
Tissue Punch 3.0 FDA UDI

Identifiers

Catalog Number
28910 FDA UDI
Primary DI / UDI-DI
07332747009408 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental soft-tissue coring punch, reusable 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 3.000 Millimeter FDA UDI

Category: Dental soft-tissue coring punch, reusable

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

Similar devices

Also classified as Dental soft-tissue coring punch, reusable.

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 327113c5-63ad-455e-b9a8-bfa755bfb642 37 fields · synced Jun 1, 2026