Compressor Nebulizer

GUDID 06950334998440

OTC-Power-AC 120V/60Hz or 220V/50Hz-Noise: 65dB

Guangdong Bestek Medical Devices Co., Ltd.

Benchtop nebulizer, non-heated

• Primary Device ID: 06950334998440
• NIH Device Record Key: 127e4789-aca4-477a-9e8f-f3ef7fcd46be
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Compressor Nebulizer
• Version Model Number: JLN-2305BS
• Company DUNS: 544095606
• Company Name: Guangdong Bestek Medical Devices Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06950334998440 [Primary]

FDA Product Code

• CAF: Nebulizer (Direct Patient Interface)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-12-15
• Device Publish Date: 2022-12-07

On-Brand Devices [Compressor Nebulizer]

• 06950334998457: OTC-Compressor flow: 8-10L Noise 65dB-Material: ABS
• 06950334998440: OTC-Power-AC 120V/60Hz or 220V/50Hz-Noise: 65dB
• 06950334998433: OTC-Compressor flow: 8-10L Noise: 65dB-Material: ABS