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Semiflexible Vessel Clamp 21cm 20mm

FDA UDI

Class II (US FDA UDI)

by Geister Medizin Technik GmbH

Identity

Trade Name
Semiflexible Vessel Clamp 21cm 20mm FDA UDI
Generic Name
Vascular clamp, reusable FDA UDI
Device Name
Semiflexible Vessel Clamp 21cm 20mm FDA UDI
Model / Reference
03-6013 FDA UDI
Description
Semiflexible Vessel Clamp 21cm 20mm FDA UDI

Identifiers

Catalog Number
03-6013 FDA UDI
Primary DI / UDI-DI
04057034014912 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Vascular clamp, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vascular clamp, reusable

Semiflexible Vessel Clamp 21cm 20mm by Geister Medizin Technik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular clamp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Geister Medizin Technik GmbH

Sources (1)

  • FDA UDI d86ac89c-1b6e-4681-8559-c4680a9e2110 35 fields · synced Jun 8, 2026