Identity
- Trade Name
- LungVision Tool FDA UDI
- Generic Name
- Bronchoscopic catheter FDA UDI
- Device Name
- The LungVision Tool is an instrument designed as a working channel intended to be used with standard bronchoscopes, endo-therapy accessories and ultrasound probe to guide the endo-therapy accessories or ultrasound probe to the target area, specifically within the respiratory system. LungVision Tool, LV2055002 is compatible with Olympus Bronchoscope BF-1T160 / BF-1T180 LungVision Tool composed from: LungVision Handle, LungVision Adaptor for Olympus Bronchoscope BF-1T160 / BF-1T180, LungVision L Curved Sheath and LungVision J Curved Wire. FDA UDI
- Model / Reference
- Bridge FDA UDI
- Description
- The LungVision Tool is an instrument designed as a working channel intended to be used with standard bronchoscopes, endo-therapy accessories and ultrasound probe to guide the endo-therapy accessories or ultrasound probe to the target area, specifically within the respiratory system. LungVision Tool, LV2055002 is compatible with Olympus Bronchoscope BF-1T160 / BF-1T180 LungVision Tool composed from: LungVision Handle, LungVision Adaptor for Olympus Bronchoscope BF-1T160 / BF-1T180, LungVision L Curved Sheath and LungVision J Curved Wire. FDA UDI
Identifiers
- Catalog Number
- LV2055002 FDA UDI
- Primary DI / UDI-DI
- 07290017652054 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
- 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
Yes
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
Category: Bronchoscopic catheter
LungVision Tool by Bodyvision Medical , Ltd. — Class II — FDA_510K — listed in FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Similar devices
Also classified as Bronchoscopic catheter.
- BroncTru™ Transbronchial Access Tool — BRONCUS MEDICAL INC. · Class II
- BroncTru™ Transbronchial Access Tool — BRONCUS MEDICAL INC. · Class II
- Ion — Intuitive Surgical, Inc. · Class II
- Edge — Covidien LP · Class II
- BroncTru™ Transbronchial Access Tool — BRONCUS MEDICAL INC. · Class II
- Edge — Covidien LP · Class II
- BroncTru™ Transbronchial Access Tool — BRONCUS MEDICAL INC. · Class II
- BroncTru™ Transbronchial Access Tool — BRONCUS MEDICAL INC. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K240943 | Class II | Active |
| FDA 510(k) | United States | FDA_510K | K163622 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bodyvision Medical , Ltd.
Sources (2)
- FDA UDI edf994d4-751a-43eb-bdb4-ec0716e5e772 58 fields · synced Jun 19, 2026
- FDA 510(k) K240943 1 fields · synced Jun 5, 2026