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Inline Sensor Assembly and Inline Temperature Sensor
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Inline Sensor Assembly and Inline Temperature Sensor FDA UDI
- Generic Name
- Pulmonary artery balloon catheter, electrical FDA UDI
- Model / Reference
- INLINE TEMPERATURE SENSOR (ILS-1) FDA UDI
Identifiers
- Catalog Number
- CA-0001-001 FDA UDI
- Primary DI / UDI-DI
- 08888893019512 FDA UDI
- FDA Product Code
- DQO FDA UDI
- GMDN Term
- Pulmonary artery balloon catheter, electrical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1200 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Inline Sensor Assembly and Inline Temperature Sensor by Bioptimal International Pte. Ltd. — Class II — FDA UDI — listed in FDA GUDID
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
- Bioptimal International Pte. Ltd.
Sources (1)
- FDA UDI 66670dc4-65a6-49be-ad66-46ecf3dc88ef 36 fields · synced May 30, 2026