Identity
- Trade Name
- LungVision SmartWire FDA UDI
- Generic Name
- Bronchoscopic catheter FDA UDI
- Device Name
- The LungVision SmartWire is an instrument designed as a stylet/wire intended to be used with 3rd party bronchoscopes and robotic bronchoscopes to mark the target area, specifically within the respiratory system FDA UDI
- Model / Reference
- Bridge FDA UDI
- Description
- The LungVision SmartWire is an instrument designed as a stylet/wire intended to be used with 3rd party bronchoscopes and robotic bronchoscopes to mark the target area, specifically within the respiratory system FDA UDI
Identifiers
- Catalog Number
- LV2055050 FDA UDI
- Primary DI / UDI-DI
- 07290017652191 FDA UDI
- 510(k) Number
- K172955 FDA UDI
- FDA Product Code
- EOQ FDA UDI
- GMDN Term
- Bronchoscopic catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.4680 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
LungVision SmartWire by Bodyvision Medical , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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
- Bodyvision Medical , Ltd.
Sources (1)
- FDA UDI cf9001f8-e687-4036-adaf-c603feb884af 36 fields · synced May 30, 2026