← Back to catalogue

Bunegin-Albin

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Bunegin-Albin FDA UDI
Generic Name
Thrombectomy suction catheter FDA UDI
Device Name
Bunegin-Albin Air Aspiration Set Polyethylene FDA UDI
Model / Reference
G05270 FDA UDI
Description
Bunegin-Albin Air Aspiration Set Polyethylene FDA UDI

Identifiers

Catalog Number
C-VAE-581J-SCJ FDA UDI
Primary DI / UDI-DI
00827002052703 FDA UDI
FDA Product Code
DXE FDA UDI
GMDN Term
Thrombectomy suction catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Thrombectomy suction catheter

Bunegin-Albin by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thrombectomy suction catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 762ba8d3-500b-4211-9b01-644a6e20dd06 36 fields · synced Jun 8, 2026