PediaPals

GUDID 06975871430048

Wenzhou Caretek Medical Device Co., Ltd.

Percussion hammer, manual, reusable

• Primary Device ID: 06975871430048
• NIH Device Record Key: 86ad3aac-15c0-4f12-a5c7-f97261042874
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PediaPals
• Version Model Number: 100009
• Company DUNS: 527815967
• Company Name: Wenzhou Caretek Medical Device Co., Ltd.
• Device Count: 1
• DM Exempt: false
• 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: false
• Lot Batch: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06975871430048 [Primary]

FDA Product Code

• FZY: Hammer, Surgical

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: 2023-03-30
• Device Publish Date: 2023-03-22

On-Brand Devices [PediaPals]

• 06975871430048: 100009
• 06975871430031: 100008