Jermei

GUDID 06972433811185

Shenzhen Jermei Medical Device Technology Co.,Ltd

Therapeutic agent nebulizer, benchtop

• Primary Device ID: 06972433811185
• NIH Device Record Key: e1d594d4-ce5c-478c-875b-cb0bc637b908
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jermei
• Version Model Number: JM838
• Company DUNS: 554534502
• Company Name: Shenzhen Jermei Medical Device Technology Co.,Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06972433811185 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K244035

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: 2026-01-09
• Device Publish Date: 2026-01-01

On-Brand Devices [Jermei]

• 06972433811079: JM821
• 06972433811109: JM828
• 06972433811192: JM839
• 06972433811185: JM838
• 06972433811130: JM832
• 06972433811123: JM830
• 06972433811086: JM822
• 06972433811062: JM818
• 06972433811055: JM817