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Konmed

FDA UDI

Class I (US FDA UDI)

by Shenzhen Konmed Technology Co., Ltd.

Identity

Trade Name
Konmed FDA UDI
Generic Name
Tubular support bandage, non-latex, reusable FDA UDI
Device Name
It is a product can be used as medical purposes specified in Intended use and it is easy to wear and take off and with humanized design, which can be adjustable in order to make effective oppression, reduce swelling and convenient for use, it is designed with below feature: - Soft and convenient to wear - Different wearing style, such as: fix on your palm and wrist, fix on your palm and fingers - Extractable aluminum alloy is, for easy cleaning and adjustment - Detachable straps to meet the needs of different person FDA UDI
Model / Reference
KM-W-19 FDA UDI
Description
It is a product can be used as medical purposes specified in Intended use and it is easy to wear and take off and with humanized design, which can be adjustable in order to make effective oppression, reduce swelling and convenient for use, it is designed with below feature: - Soft and convenient to wear - Different wearing style, such as: fix on your palm and wrist, fix on your palm and fingers - Extractable aluminum alloy is, for easy cleaning and adjustment - Detachable straps to meet the needs of different person FDA UDI

Identifiers

Primary DI / UDI-DI
06970935830239 FDA UDI
FDA Product Code
ILH FDA UDI
GMDN Term
Tubular support bandage, non-latex, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tubular support bandage, non-latex, reusable

Konmed by Shenzhen Konmed Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tubular support bandage, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 187918f7-5fcd-4709-b907-7649031ea69e 33 fields · synced May 30, 2026