NeoDevices, Inc. ND24EF-HF

by Neodevices Inc

NeoDevices, Inc. ND24EF-HF is a Class II device made by Neodevices Inc, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10816340021554), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10816340021554 UDI-DI	Date24 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10816340021554

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: NeoDevices, Inc.
Generic name: Intravenous administration tubing extension set
Model / reference: ND24EF-HF
Description: 24" High Flow Orange Stripe Extension set with EnFit Connectors (ISO 80369 compatible)

Primary DI / UDI-DI: 10816340021554
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

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Properties

Supplied sterile
Single use
Prescription use
Lot / batch number

Other properties (11, all answered No)