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Medusa Multi-Coil MMC-120

by Endoshape, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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 Number10857798005000 UDI-DI Date23 Sep 2015ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Medusa Multi-Coil
Generic Name
Non-neurovascular embolization coil
Model / Ref / Catalog
MMC-120, 002155
Primary DI / UDI-DI
10857798005000
FDA Product Code
KRD
GMDN Term
Non-neurovascular embolization coil
Device Class
Class II
Regulation Number
870.3300
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Conditional

Other devices from Endoshape, Inc.

Properties

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

Other properties (8)

  • 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