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Nester G31459

by Cook Incorporated

Nester G31459 (MWCE-38-8-8-NESTER) is a Class II device made by Cook Incorporated, listed in FDA GUDID since 24 Oct 2015 (UDI-DI 00827002314597), 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 Number00827002314597 UDI-DI Date24 Oct 2015ListedStatusListed 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  • Withdrawn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
Nester
Generic name
Non-neurovascular embolization coil
Model / Ref / Catalog
G31459, MWCE-38-8-8-NESTER
Primary DI / UDI-DI
00827002314597
FDA product code
KRD
GMDN term
Non-neurovascular embolization coil
Device class
Class II
Regulation number
870.3300
GUDID distribution status
In Commercial Distribution

Related devices

Category: Non-neurovascular embolization coil

Similar devices in this category

Other devices filed under Non-neurovascular embolization coil.

Other devices from Cook Incorporated

See all devices from Cook Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)