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Bailey Aortic Clamp angled 21cm 30x8 shanks curved

FDA UDI

Class II (US FDA UDI)

by Geister Medizin Technik GmbH

Identity

Trade Name
Bailey Aortic Clamp angled 21cm 30x8 shanks curved FDA UDI
Generic Name
Vascular clamp, reusable FDA UDI
Device Name
Bailey Aortic Clamp angled 21cm 30x8 shanks curved FDA UDI
Model / Reference
22-0421 FDA UDI
Description
Bailey Aortic Clamp angled 21cm 30x8 shanks curved FDA UDI

Identifiers

Catalog Number
22-0421 FDA UDI
Primary DI / UDI-DI
04057034055847 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

Bailey Aortic Clamp angled 21cm 30x8 shanks curved 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 861d5f97-2f6c-4336-9890-892b057b0c5e 35 fields · synced May 30, 2026