Disposable Grounding Pad Series

GUDID 06924274955351

Zhejiang Shuyou Surgical Instrument Co.,Ltd.

Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile Electrosurgical return electrode, single-use, sterile

• Primary Device ID: 06924274955351
• NIH Device Record Key: e826d7f3-0cce-4505-bf03-cb263e3ce447
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Disposable Grounding Pad Series
• Version Model Number: SY-M4
• Company DUNS: 421340711
• Company Name: Zhejiang Shuyou Surgical Instrument 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	06924274955351 [Primary]
GS1	06924274955368 [Package]; Package: [40 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091672

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-03-10

On-Brand Devices [Disposable Grounding Pad Series]

• 06924274955405: SY-MW4
• 06924274955351: SY-M4
• 06924274951780: P4500
• 06924274930099: SY-C2
• 06924274930082: SY-C1
• 06924274920243: SY-BW4
• 06924274920236: SY-BW3
• 6924274921004: SY-BW2
• 06924274920212: SY-BW1
• 06924274920205: SY-SW4
• 06924274920199: SY-SW3
• 6924274920854: SY-SW2
• 6924274920809: SY-SW1
• 6924274920601: SY-MW3
• 6924274920557: SY-MW2
• 6924274920502: SY-MW1
• 06924274920120: SY-B4
• 06924274920113: SY-B3
• 6924274920953: SY-B2
• 6924274920908: SY-B1
• 06924274920083: SY-S4
• 06924274920076: SY-S3
• 6924274920755: SY-S2
• 6924274920700: SY-S1
• 6924274920403: SY-M3
• 6924274920359: SY-M2
• 6924274920304: SY-M1