Sunmed Inflation Device

GUDID 06947358566007

Sunny Medical Device (Shenzhen) Co., Ltd.

Catheter/overtube balloon inflator, single-use

• Primary Device ID: 06947358566007
• NIH Device Record Key: c814d7a4-aa97-49f0-80e5-e0bcc0898421
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sunmed Inflation Device
• Version Model Number: J Type, 28ml, 30atm/bar
• Company DUNS: 529639795
• Company Name: Sunny Medical Device (Shenzhen) 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: 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	06947358566007 [Primary]

FDA Product Code

• PTM: Syringe, Balloon Inflation, 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: 2022-01-12
• Device Publish Date: 2022-01-04

On-Brand Devices [Sunmed Inflation Device]

• 06947358563006: 30atm, 30ml
• 06947358568001: J Type, 28ml, 40atm/bar
• 06947358566007: J Type, 28ml, 30atm/bar