← Back to catalogue

Goben

FDA UDI

Class I (US FDA UDI)

by Huzhou Junda Industry Co., Ltd.

Identity

Trade Name
GOBEN FDA UDI
Generic Name
Pressure bandage, non-latex, single-use FDA UDI
Device Name
Elastic Bandages with Self Closure - 4 in x 5 yds, Color: White/beige Closure Type: Velcro FDA UDI
Model / Reference
JD01-B010203 FDA UDI
Description
Elastic Bandages with Self Closure - 4 in x 5 yds, Color: White/beige Closure Type: Velcro FDA UDI

Identifiers

Primary DI / UDI-DI
06979032640109 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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

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: Pressure bandage, non-latex, single-use

Goben by Huzhou Junda Industry Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure bandage, non-latex, single-use.

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

Sources (1)

  • FDA UDI 154334f6-6f10-456b-8b43-4a0909cd69da 33 fields · synced May 30, 2026