Neoscope NBF 50
by Prosurg, Inc
Neoscope NBF 50 is a Class II device made by Prosurg, Inc, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00851545007562), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00851545007562 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00851545007562
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Neoscope
- Generic name
- Flexible video bronchoscope, single-use
- Model / reference
- NBF 50
- Primary DI / UDI-DI
- 00851545007562
- FDA product code
- EOQ
- GMDN term
- Flexible video bronchoscope, single-use
- Device class
- Class II
- Regulation number
- 874.4680
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 5.0 Millimeter
Similar devices in this category
Other devices filed under Flexible video bronchoscope, single-use.
- aScope™ 4 Broncho Regular 5.0/2.2 477001000 by Ambu A/S
- aScope™ 4 Broncho Large Sampler Set 5.8/2.8 478501000 by Ambu A/S
- LoopView® B50-C by MacroLux Medical Technology Co., Ltd.
- Ion 490206 by Intuitive Surgical, Inc.
- BFlex™ 2 Slim 3.8 0570-0432 by Verathon Medical (Canada) ULC
- LoopView® B58-C by MacroLux Medical Technology Co., Ltd.
- Single-Use Video Bronchoscope SVB11001 by Micro-Tech (Nanjing) Co., Ltd.
- BFlex™ 2 Large 5.8 0570-0424 by Verathon Medical (Canada) ULC