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Excelsior Reach MC17PS90155-01

by Stryker Corp.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 9 Nov 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 9 Nov 2026. What this means

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07613327682434 UDI-DI Date29 Oct 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 9 Nov 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Excelsior Reach
Generic name
Vascular microcatheter
Model / Ref / Catalog
MC17PS90155-01
Primary DI / UDI-DI
07613327682434
510(k) Number
FDA product code
DQY, QJP
GMDN term
Vascular microcatheter
Device class
Class II
Regulation number
870.1250
GUDID distribution status
In Commercial Distribution
Size
Length — 155.0 Centimeter
Lumen/Inner Diameter — 0.0165 Inch

Related devices

Cleared under the same submission (K261649)

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date

Other properties (10)

  • Sterilise before use: No
  • 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