← Back to catalogue

Helmut Zepf

FDA UDI

Class I (US FDA UDI)

by Helmut Zepf Medizintechnik GmbH

Identity

Trade Name
HELMUT ZEPF FDA UDI
Generic Name
Dental elevator, tooth/root FDA UDI
Device Name
CHISEL, BONE ROTARY CHISEL, MOD. VIENNA, BAYONET 5MM, FIG. 5B FLAT HANLDE FDA UDI
Model / Reference
41.541.05WM FDA UDI
Description
CHISEL, BONE ROTARY CHISEL, MOD. VIENNA, BAYONET 5MM, FIG. 5B FLAT HANLDE FDA UDI

Identifiers

Catalog Number
41.541.05WM FDA UDI
Primary DI / UDI-DI
EZPF4154105WM0 FDA UDI
FDA Product Code
EML FDA UDI
GMDN Term
Dental elevator, tooth/root 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental elevator, tooth/root

Helmut Zepf by Helmut Zepf Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental elevator, tooth/root.

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

Sources (1)

  • FDA UDI d5c0477c-8f48-4bf5-8cda-33d7b4ba1abb 35 fields · synced May 30, 2026