hypodermic needles

GUDID 06949236202496

Berpu Medical Technology Co.,Ltd

Hypodermic needle, single-use

• Primary Device ID: 06949236202496
• NIH Device Record Key: e32930b0-188a-4ff1-8874-25b2042612c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: hypodermic needles
• Version Model Number: 25G×38mmRW
• Company DUNS: 529239746
• Company Name: Berpu Medical 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06949236202489 [Primary]
GS1	06949236202496 [Package]; Contains: 06949236202489; Package: [100 Units]; In Commercial Distribution
GS1	06949236202502 [Package]; Package: [40 Units]; In Commercial Distribution

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-10-20
• Device Publish Date: 2020-10-12

On-Brand Devices [hypodermic needles]

• 06949236202311: 30G×13mmRW
• 06949236202342: 23G×38mmTW
• 06949236202526: 25G×25mmRW
• 06949236202496: 25G×38mmRW
• 06949236202465: 22G×38mmTW
• 06949236202434: 21G×38mmTW
• 06949236202403: 20G×38mmTW
• 06949236202373: 19G×38mmTW