Identity
- Trade Name
- Redi Splint FDA UDI
- Generic Name
- First aid limb splint, mouldable, single-use FDA UDI
- Device Name
- Redi Universal Splint, Small, Olive Drab, Flat. Moldable first aid splint. FDA UDI
- Model / Reference
- Redi Universal Splint FDA UDI
- Description
- Redi Universal Splint, Small, Olive Drab, Flat. Moldable first aid splint. FDA UDI
Identifiers
- Catalog Number
- 1211321 FDA UDI
- Primary DI / UDI-DI
- B54112113210 FDA UDI
- FDA Product Code
- NOC FDA UDI
- GMDN Term
- First aid limb splint, mouldable, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.3910 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: First aid limb splint, mouldable, single-use
Redi Splint by Faretec, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as First aid limb splint, mouldable, single-use.
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- Tealmed — Ningbo Tealmed Emergency Products Co., Ltd. · Class I
- Prometheus Omni Splint Flat — SAFEGUARD MEDICAL TECHNOLOGIES LIMITED · Class I
- Tealmed — Ningbo Tealmed Emergency Products Co., Ltd. · Class I
- EMSRUN — Wuxi Emsrun Technology 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
- Faretec, Inc.
Sources (1)
- FDA UDI 1a41c96f-3b35-45b7-8086-961482a9f783 35 fields · synced Jun 6, 2026