Identity
- Trade Name
- Curaplex FDA UDI
- Generic Name
- First aid kit, non-medicated, single-use FDA UDI
- Device Name
- State of Nevada OEMS Pediatric ALS FDA UDI
- Model / Reference
- 8600-01393 FDA UDI
- Description
- State of Nevada OEMS Pediatric ALS FDA UDI
Identifiers
- Catalog Number
- 8600-01393 FDA UDI
- Primary DI / UDI-DI
- 00812277035100 FDA UDI
- FDA Product Code
- CAT FDA UDILDE FDA UDIBTM FDA UDICAE FDA UDICCK FDA UDIFPK FDA UDIFPA FDA UDILRS FDA UDIFMI FDA UDIKGB FDA UDIFOZ FDA UDIDRX FDA UDIFMF FDA UDIMMK FDA UDIJOL FDA UDIBYG FDA UDIDXQ FDA UDINOD FDA UDIGAA FDA UDI
- GMDN Term
- First aid kit, non-medicated, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5340 FDA UDI870.1875 FDA UDI868.5915 FDA UDI868.5110 FDA UDI868.1400 FDA UDI880.5440 FDA UDI880.5200 FDA UDI880.5570 FDA UDI868.5570 FDA UDI870.2360 FDA UDI880.5860 FDA UDI880.6740 FDA UDI868.5580 FDA UDI870.1120 FDA UDI878.3910 FDA UDI878.4800 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: First aid kit, non-medicated, single-use
Curaplex by Bound Tree Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Bound Tree Medical, Llc
Sources (1)
- FDA UDI c8f32ca5-aa8b-4309-8e41-1bb231d6f2fe 34 fields · synced May 30, 2026