Identity
- Trade Name
- seca 404 FDA UDI
- Generic Name
- Fixed ramp FDA UDI
- Device Name
- The ramp is intended to enable the clinical staff to push a patient's wheelchair, bed or stretcher onto the platform of a compatible electronic platform scale. FDA UDI
- Model / Reference
- 404 FDA UDI
- Description
- The ramp is intended to enable the clinical staff to push a patient's wheelchair, bed or stretcher onto the platform of a compatible electronic platform scale. FDA UDI
Identifiers
- Catalog Number
- 4040000009 FDA UDI
- Primary DI / UDI-DI
- 04012030021593 FDA UDI
- FDA Product Code
- FRW FDA UDI
- GMDN Term
- Fixed ramp FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.2720 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Fixed ramp
seca 404 by Seca Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Fixed ramp.
- seca 405 — Seca Corp. · 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
- Seca Corp.
Sources (1)
- FDA UDI 1c31a212-4324-4895-a6b7-21003a86b347 35 fields · synced Jun 1, 2026