Identity
- Trade Name
- Curaplex FDA UDI
- Generic Name
- Transcutaneous blood gas monitor sensor FDA UDI
- Device Name
- BTM Light Weight Monitoring Module / ECG, RESP, NPB, SPO2, P+T FDA UDI
- Model / Reference
- 2525-13623 FDA UDI
- Description
- BTM Light Weight Monitoring Module / ECG, RESP, NPB, SPO2, P+T FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815277020602 FDA UDI
- FDA Product Code
- DSA FDA UDIPFY FDA UDIDXQ FDA UDIBZT FDA UDI
- GMDN Term
- Transcutaneous blood gas monitor sensor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2900 FDA UDI870.2300 FDA UDI870.1120 FDA UDI868.1920 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
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Blood pressure cuff, reusableGeneral-purpose patient temperature probe, single-useTranscutaneous blood gas monitor sensorIntracardiac oximeter
Curaplex by Bound Tree Medical, Llc — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Bound Tree Medical, Llc
Sources (1)
- FDA UDI 919e44a6-6d0e-4ca6-adeb-ae81a202085f 33 fields · synced Jun 6, 2026