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Compressor Nebulizer JLN-2305BS

by Guangdong Bestek Medical Devices Co., Ltd. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06950334998440 UDI-DIDate7 Dec 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Compressor Nebulizer
Generic Name
Therapeutic agent nebulizer, benchtop
Model / Reference
JLN-2305BS
Description
OTC-Power-AC 120V/60Hz or 220V/50Hz-Noise: 65dB
Primary DI / UDI-DI
06950334998440
FDA Product Code
CAF
GMDN Term
Therapeutic agent nebulizer, benchtop
Device Class
Class II
Regulation Number
868.5630
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Related devices

Category: Therapeutic agent nebulizer, benchtop

Other devices from Guangdong Bestek Medical Devices Co., Ltd.

Properties

  • Over-the-Counter
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No