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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
Periosteal elevator, reusable FDA UDI
Device Name
BONE PLUGGER, DOUBLE-ENDED Ø 3MM / Ø 5MM, CROSS-SERRATED, STAINLESS STEEL HANDLE FDA UDI
Model / Reference
47.848.04 FDA UDI
Description
BONE PLUGGER, DOUBLE-ENDED Ø 3MM / Ø 5MM, CROSS-SERRATED, STAINLESS STEEL HANDLE FDA UDI

Identifiers

Catalog Number
47.848.04 FDA UDI
Primary DI / UDI-DI
EZPF47848040 FDA UDI
FDA Product Code
KXF FDA UDI
GMDN Term
Periosteal elevator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6025 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: Periosteal elevator, reusable

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

Similar devices

Also classified as Periosteal elevator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI afcbd73a-3be7-4e74-bb91-90fe74c0a976 35 fields · synced May 30, 2026