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CORLO Twoomey 30-6216

by Corpak Medsystems

CORLO Twoomey 30-6216 is a Class II device made by Corpak Medsystems, listed in FDA GUDID since 4 Aug 2016 (UDI-DI 10815149024179), 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 Number10815149024179 UDI-DI Date4 Aug 2016ListedStatusListed 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  • Withdrawn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
CORLO Twoomey
Generic name
Jejunostomy tube
Model / Ref / Catalog
30-6216
Primary DI / UDI-DI
10815149024179
FDA product code
KNT
GMDN term
Jejunostomy tube
Device class
Class II
Regulation number
876.5980
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 16 French

Similar devices

Other devices filed under FDA product code KNT (TUBES, GASTROINTESTINAL (AND ACCESSORIES)).

Other devices from Corpak Medsystems

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Properties

  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)