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NeoBottle SSNB-CL

by Neomed, Inc.

NeoBottle SSNB-CL is a Class I device made by Neomed, Inc., listed in FDA GUDID since 19 Sep 2016 (UDI-DI 00817584010222), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817584010222 UDI-DI Date19 Sep 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  • Withdrawn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
NeoBottle
Generic name
ENFit oral/enteral syringe, single-use
Model / Ref / Catalog
SSNB-CL
Primary DI / UDI-DI
00817584010222
FDA product code
KYX
GMDN term
ENFit oral/enteral syringe, single-use
Device class
Class I
Regulation number
880.6430
GUDID distribution status
In Commercial Distribution

Related devices

Category: ENFit oral/enteral syringe, single-use

Similar devices in this category

Other devices filed under ENFit oral/enteral syringe, single-use.

Other devices from Neomed, Inc.

See all devices from Neomed, Inc. →

Properties

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