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Evis Eus Ultrasound Bronchofibervideoscope Olympus Bf-UCP190F

by Olympus Medical Systems Corporation

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04953170440410 UDI-DI Date9 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Evis Eus Ultrasound Bronchofibervideoscope
Generic Name
Flexible ultrasound bronchoscope
Model / Ref / Catalog
OLYMPUS BF-UCP190F, N6131340
Primary DI / UDI-DI
04953170440410
510(k) Number
FDA Product Code
PSV, ITX
GMDN Term
Flexible ultrasound bronchoscope
Device Class
Class II
Regulation Number
892.1550, 892.1570
GUDID distribution status
In Commercial Distribution

Other devices from Olympus Medical Systems Corporation

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Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No