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Target M0036180630

by Stryker Corp.

Target M0036180630 is a Class II device made by Stryker Corp., listed in FDA GUDID since 5 Sep 2019 (UDI-DI 07613327466393), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07613327466393 UDI-DI Date5 Sep 2019ListedStatusListed 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  • Withdrawn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
Target
Generic name
Non-neurovascular embolization coil
Model / Ref / Catalog
M0036180630, 618063
Primary DI / UDI-DI
07613327466393
FDA product code
KRD, HCG
GMDN term
Non-neurovascular embolization coil
Device class
Class II
Regulation number
870.3300, 882.5950
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Neurovascular embolization coilNon-neurovascular embolization coil

Similar devices in this category

Other devices filed under Non-neurovascular embolization coil.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)