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CleanCapture Aspiration Catheter 2189

by Hobbs Medical, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM84921890 UDI-DI Date14 Jan 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
CleanCapture Aspiration Catheter
Generic Name
Suction system catheter, general-purpose
Model / Ref / Catalog
2189
Primary DI / UDI-DI
M84921890
510(k) Number
FDA Product Code
OCX
GMDN Term
Suction system catheter, general-purpose
Device Class
Class II
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 2.77 Millimeter
Catheter Working Length — 160 Centimeter

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Properties

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

Other properties (8)

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