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NeoDevices, Inc. ND-BF20

by Neodevices Inc

NeoDevices, Inc. ND-BF20 is a Class II device made by Neodevices Inc, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10816340022117), 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 Number10816340022117 UDI-DI Date24 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  • Withdrawn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
NeoDevices, Inc.
Generic name
Blood transfusion filter
Model / reference
ND-BF20
Primary DI / UDI-DI
10816340022117
FDA product code
FPA
GMDN term
Blood transfusion filter
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood transfusion filter

Other devices from Neodevices Inc

See all devices from Neodevices Inc →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)