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ND60EL-Hf

by Neodevices Inc

ND60EL-Hf is a Class II device made by Neodevices Inc, listed in FDA GUDID since 13 Oct 2026 (UDI-DI 00816340021663), 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 Number00816340021663 UDI-DI Date13 Oct 2026ListedStatusListed 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  • Withdrawn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

Generic name
Intravenous administration tubing extension set
Model / reference
ND60EL-HF
Description
60" High Flow Orange Stripe Extension set with Enteral Locking Connectors (ISO 80369 compatible) Priming Vol approx 10ml
Primary DI / UDI-DI
00816340021663
FDA product code
KNT
GMDN term
Intravenous administration tubing extension set
Device class
Class II
Regulation number
876.5980
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KNT (Tubes, Gastrointestinal (And Accessories)).

Other devices from Neodevices Inc

See all devices from Neodevices Inc →

Properties

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