Identity
- Trade Name
- EVERYWAY4ALL FDA UDI
- Generic Name
- Vertical non-powered traction system FDA UDI
- Device Name
- Apparatus, traction, non-powered FDA UDI
- Model / Reference
- CT-800 FDA UDI
- Description
- Apparatus, traction, non-powered FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04719871180167 FDA UDI
- FDA Product Code
- HST FDA UDI
- GMDN Term
- Vertical non-powered traction system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.5850 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Category: Vertical non-powered traction system
Everyway4all by Everyway Medical Instruments Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vertical non-powered traction system.
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- EVERYWAY4ALL — EVERYWAY MEDICAL INSTRUMENTS CO., LTD. · 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
- Everyway Medical Instruments Co., Ltd.
Sources (1)
- FDA UDI 87578211-2e1f-498c-8841-ba897207aea2 33 fields · synced Jun 8, 2026