Nebulizer

GUDID 06950334998426

OTC-Power-AC 120V 60Hz or 220V 50Hz-Material: ABS

Guangdong Bestek Medical Devices Co., Ltd.

Benchtop nebulizer, non-heated

• Primary Device ID: 06950334998426
• NIH Device Record Key: d7a484b0-d223-44c1-a48a-195a60ad3127
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nebulizer
• Version Model Number: JLN-2322AS
• 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	06950334998426 [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 [Nebulizer]

• 06950334998426: OTC-Power-AC 120V 60Hz or 220V 50Hz-Material: ABS
• 06950334998419: OTC-Power-AC 120V 60Hz or 220V 50Hz-Noise 65dB
• 06950334998402: OTC-Power-AC 120V/60Hz or 220V/50Hz-Material: ABS