Denudation Pipettes

GUDID 06972598791889

Guangzhou PINZHI Medical Device Co., Ltd.

User-induced micropipette

• Primary Device ID: 06972598791889
• NIH Device Record Key: 8d59b71e-210c-469e-845a-029db3b749f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Denudation Pipettes
• Version Model Number: S-P-PD150/10
• Company DUNS: 418527269
• Company Name: Guangzhou PINZHI Medical Device Co., Ltd.
• Device Count: 10
• DM Exempt: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06972598791889 [Primary]
GS1	16972598791886 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K250838

FDA Product Code

• MQH: Microtools, Assisted Reproduction (Pipettes)

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: 2025-12-23
• Device Publish Date: 2025-12-15

On-Brand Devices [Denudation Pipettes]

• 06972598791902: S-P-PD290/10
• 06972598791896: S-P-PD170/10
• 06972598791889: S-P-PD150/10
• 06972598791872: S-P-PD140/10