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Punches, NOBEL

FDA UDI

Class I (US FDA UDI)

by Omnia Spa

Identity

Trade Name
Punches, NOBEL FDA UDI
Generic Name
Dental soft-tissue coring punch, single-use FDA UDI
Device Name
Soft Tissue Punch Ø 4.1 mm, 5-pack FDA UDI
Model / Reference
32.Z2000.00 FDA UDI
Description
Soft Tissue Punch Ø 4.1 mm, 5-pack FDA UDI

Identifiers

Primary DI / UDI-DI
08056646504770 FDA UDI
FDA Product Code
EME FDA UDI
GMDN Term
Dental soft-tissue coring punch, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

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

Yes

FDA UDI

Category: Dental soft-tissue coring punch, single-use

Punches, NOBEL by Omnia Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental soft-tissue coring punch, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Omnia Spa

Sources (1)

  • FDA UDI a32cbd54-1cff-479a-8575-98201d1ed04e 33 fields · synced May 30, 2026