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MicroPlex Cosmos 100837CSSR-V

by Microvention Inc.

MicroPlex Cosmos 100837CSSR-V is a Class II device made by Microvention Inc., listed in FDA GUDID since 7 Aug 2018 (UDI-DI 00810170013591), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810170013591 UDI-DI Date7 Aug 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
MicroPlex Cosmos
Generic name
Neurovascular embolization coil
Model / Ref / Catalog
100837CSSR-V
Primary DI / UDI-DI
00810170013591
FDA product code
HCG
GMDN term
Neurovascular embolization coil
Device class
Class II
Regulation number
882.5950
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Neurovascular embolization coil

Similar devices

Other devices filed under FDA product code HCG (DEVICE, NEUROVASCULAR EMBOLIZATION).

Other devices from Microvention Inc.

See all devices from Microvention Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)