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Lazic

FDA UDI

Class I (US FDA UDI)

by Peter Lazic GmbH

Identity

Trade Name
LAZIC FDA UDI
Generic Name
Surgical A/V-shaped microvessel clamp FDA UDI
Device Name
MICRO SINGLE CLAMP FOR VEIN LENGTH 36 MM; Ø VESSEL 2,0 - 5,0 MM PU 2 PCS / CODE: RD-S 5V FDA UDI
Model / Reference
64.405.01 FDA UDI
Description
MICRO SINGLE CLAMP FOR VEIN LENGTH 36 MM; Ø VESSEL 2,0 - 5,0 MM PU 2 PCS / CODE: RD-S 5V FDA UDI

Identifiers

Catalog Number
64.405.01 FDA UDI
Primary DI / UDI-DI
04250603711643 FDA UDI
FDA Product Code
HXD FDA UDI
GMDN Term
Surgical A/V-shaped microvessel clamp 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: Surgical A/V-shaped microvessel clamp

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

Similar devices

Also classified as Surgical A/V-shaped microvessel clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Peter Lazic GmbH

Sources (1)

  • FDA UDI 5e4d1c34-66c3-49d8-92f5-afce8c398eb8 35 fields · synced May 30, 2026