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Digital MurphyScope Endoscope 2125-515

by Clarus Medical, LLC

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 Number00810004821118 UDI-DI Date21 Apr 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  • Withdrawn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
Digital MurphyScope Endoscope
Generic Name
Rigid video intracranial/spinal endoscope
Model / Ref / Catalog
2125-515
Primary DI / UDI-DI
00810004821118
510(k) Number
FDA Product Code
GWG
GMDN Term
Rigid video intracranial/spinal endoscope
Device Class
Class II
Regulation Number
882.1480
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K223615)

Show all (11)

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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