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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 ARTERY LENGTH 8 MM; Ø VESSEL 0,3 - 0,8 MM (=1pair) / CODE: B-1A, CLASSIC STYLE FDA UDI
Model / Reference
64.411.21 FDA UDI
Description
MICRO SINGLE CLAMP FOR ARTERY LENGTH 8 MM; Ø VESSEL 0,3 - 0,8 MM (=1pair) / CODE: B-1A, CLASSIC STYLE FDA UDI

Identifiers

Catalog Number
64.411.21 FDA UDI
Primary DI / UDI-DI
04250603744849 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 271b710f-7075-4fd3-a498-0224d96251a0 35 fields · synced Jun 8, 2026