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Aortic Clamp

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
Aortic Clamp FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI
Device Name
Debakey Straight Aortic Clamp 9.5" FDA UDI
Model / Reference
Debakey Straight FDA UDI
Description
Debakey Straight Aortic Clamp 9.5" FDA UDI

Identifiers

Catalog Number
505249 FDA UDI
Primary DI / UDI-DI
B9745052490 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 9.5 Inch FDA UDI

Category: Surgical soft-tissue manipulation forceps, tweezers-like, single-use

Aortic Clamp by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, tweezers-like, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dr.frigz International(pvt)ltd,

Sources (1)

  • FDA UDI 7983327f-5827-44d0-9bc5-d32214a69b8a 35 fields · synced May 30, 2026