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Single Use Guiding Device CC-220DR

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 Number04953170406171 UDI-DI Date7 Sep 2021ListedStatusListed 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  • Withdrawn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
Single Use Guiding Device
Generic Name
Bronchoscopic biopsy curette, flexible, single-use
Model / Reference
CC-220DR
Primary DI / UDI-DI
04953170406171
510(k) Number
FDA Product Code
BTG, EOQ
GMDN Term
Bronchoscopic biopsy curette, flexible, single-use
Device Class
Class II
Regulation Number
874.4680
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bronchoscopic biopsy curette, flexible, single-use

Other devices from Olympus Medical Systems Corporation

See all devices from Olympus Medical Systems Corporation →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No