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, with adjustable size which will not affected by the size of your hands. FDA UDI
- Model / Reference
- KM-W-40 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, with adjustable size which will not affected by the size of your hands. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06970935830246 FDA UDI
- FDA Product Code
- LQX 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.
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- MediChoice — OWENS & MINOR DISTRIBUTION, INC. · Class I
- Tubifast® — Mölnlycke Health Care AB · Class I
- Tubifast® — Mölnlycke Health Care AB · Class I
- WALGREENS — WALGREEN CO. · Class I
- ViveCare — VIVE HEALTH LLC · Class I
- Juzo Suspension Sleeve — JULIUS ZORN, INC. · Class I
- MediChoice — OWENS & MINOR DISTRIBUTION, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Shenzhen Konmed Technology Co., Ltd.
Sources (1)
- FDA UDI 8e804797-0d34-45f9-9982-8d754fc6a30b 33 fields · synced May 30, 2026