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Helmut Zepf

FDA UDI

Class I (US FDA UDI)

by Helmut Zepf Medizintechnik GmbH

Identity

Trade Name
HELMUT ZEPF FDA UDI
Generic Name
Wire holding/twisting pliers FDA UDI
Device Name
PLIER, ORTHODONTIC DIAMOND TIPS ONLY, RIGID, 2.35 MM, 31.185.00, 31.185.01,31.185.04 FDA UDI
Model / Reference
31.185.12 FDA UDI
Description
PLIER, ORTHODONTIC DIAMOND TIPS ONLY, RIGID, 2.35 MM, 31.185.00, 31.185.01,31.185.04 FDA UDI

Identifiers

Catalog Number
31.185.12 FDA UDI
Primary DI / UDI-DI
EZPF31185120 FDA UDI
FDA Product Code
JEX FDA UDI
GMDN Term
Wire holding/twisting pliers 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: Wire holding/twisting pliers

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

Similar devices

Also classified as Wire holding/twisting pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Helmut Zepf Medizintechnik GmbH

Sources (1)

  • FDA UDI e2469fcb-162c-4ace-bcf7-68f68e53f7e0 35 fields · synced Jun 8, 2026