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Goben

FDA UDI

Class II (US FDA UDI)

by Huzhou Junda Industry Co., Ltd.

Identity

Trade Name
GOBEN FDA UDI
Generic Name
Thrombectomy suction catheter FDA UDI
Device Name
First Call Hi-Vac Aspiration Tubing, 9',High Vac Aspiration Tubing,High Flow,Latex Free Reduced “memory”,Sterile, Length: 9ft,Internal Diameter: 3/8 in. FDA UDI
Model / Reference
JD12-U030101 FDA UDI
Description
First Call Hi-Vac Aspiration Tubing, 9',High Vac Aspiration Tubing,High Flow,Latex Free Reduced “memory”,Sterile, Length: 9ft,Internal Diameter: 3/8 in. FDA UDI

Identifiers

Primary DI / UDI-DI
06979032640017 FDA UDI
FDA Product Code
BYY FDA UDI
GMDN Term
Thrombectomy suction catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

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

Goben by Huzhou Junda Industry Co., Ltd. — 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

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Manufacturer

Sources (1)

  • FDA UDI 7250cdde-15d1-49c9-9397-339bbd994f1b 33 fields · synced Jun 6, 2026