Biopsy pipettes

GUDID 06972598791865

Guangzhou PINZHI Medical Device Co., Ltd.

User-induced micropipette

• Primary Device ID: 06972598791865
• NIH Device Record Key: b34a7c90-d4be-4a29-8df2-7e0c763b9676
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Biopsy pipettes
• Version Model Number: S-P-B35.30
• Company DUNS: 418527269
• Company Name: Guangzhou PINZHI Medical Device Co., Ltd.
• Device Count: 10
• DM Exempt: true
• Pre-market Exempt: true
• 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	06972598791865 [Primary]
GS1	16972598791862 [Unit of Use]

FDA Product Code

• PUC: Microtools, Assisted Reproduction (Pipettes), Exempt

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

Devices Manufactured by Guangzhou PINZHI Medical Device Co., Ltd.

• 06972598791865 - Biopsy pipettes: 2025-12-23
• 06972598791865 - Biopsy pipettes: 2025-12-23
• 06972598791872 - Denudation Pipettes: 2025-12-23
• 06972598791889 - Denudation Pipettes: 2025-12-23
• 06972598791896 - Denudation Pipettes: 2025-12-23
• 06972598791902 - Denudation Pipettes: 2025-12-23