Identity
- Trade Name
- Savoy QA3 FDA UDI
- Generic Name
- Orthopaedic stretcher FDA UDI
- Model / Reference
- 7QA3MES FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815871020589 FDA UDI
- FDA Product Code
- FPO FDA UDI
- GMDN Term
- Orthopaedic stretcher FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6910 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
No
FDA UDI
Category: Orthopaedic stretcher
Savoy QA3 by Avante — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic stretcher.
- Sechrist Industries, Inc. — Sechrist Industries Inc · Class II
- Sechrist Industries, Inc. — Sechrist Industries Inc · Class II
- Sechrist Industries, Inc. — Sechrist Industries Inc · Class II
- ADVANCED STRETCHER, HAND-CARRIED — ADVANCED INSTRUMENTATIONS, INC. · Class I
- Sechrist Industries, Inc. — Sechrist Industries Inc · Class II
- Sechrist Industries, Inc. — Sechrist Industries Inc · Class II
- Sechrist Industries, Inc. — Sechrist Industries Inc · Class II
- Sechrist Industries, Inc. — Sechrist Industries Inc · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Avante
Sources (1)
- FDA UDI 0440bc75-b001-489c-a5c9-00b6ba4b4eca 33 fields · synced Jun 8, 2026