← Back to catalogue

Lazic

FDA UDI

Class I (US FDA UDI)

by Peter Lazic GmbH

Identity

Trade Name
LAZIC FDA UDI
Generic Name
Vessel approximator FDA UDI
Device Name
BIEMER-MÜLLER Approximators 5x9mm angled 45°, Clos.force 25-30gms. FDA UDI
Model / Reference
64.612 FDA UDI
Description
BIEMER-MÜLLER Approximators 5x9mm angled 45°, Clos.force 25-30gms. FDA UDI

Identifiers

Catalog Number
64.612 FDA UDI
Primary DI / UDI-DI
04250603710295 FDA UDI
FDA Product Code
HXD FDA UDI
GMDN Term
Vessel approximator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Category: Vessel approximator

Lazic by Peter Lazic GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vessel approximator.

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

Manufacturer
Peter Lazic GmbH

Sources (1)

  • FDA UDI a045feb7-ec2d-494f-a5a1-bf651353a0de 35 fields · synced May 30, 2026