Peng’s Multifunctional Operative Dissector(PMOD)

GUDID 16924274957161

Zhejiang Shuyou Surgical Instrument Co.,Ltd.

Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use

• Primary Device ID: 16924274957161
• NIH Device Record Key: 6806902d-cae7-4075-a250-32852cfbe35d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Peng’s Multifunctional Operative Dissector(PMOD)
• Version Model Number: ISEP1000
• 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	06924274957164 [Primary]
GS1	16924274957161 [Package]; Contains: 06924274957164; Package: [5 Units]; In Commercial Distribution
GS1	26924274957168 [Package]; Contains: 06924274957164; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K040780

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2020-07-27
• Device Publish Date: 2020-07-17

On-Brand Devices [Peng’s Multifunctional Operative Dissector(PMOD)]

• 06924274956075: IIIA-D602-SG365
• 06924274956020: IIIA-D602-SG365
• 06924274955979: IIIA-D006-SG040
• 06924274955917: IIIA-D006-SG039
• 06924274955542: 8230
• 06924274953685: P0035H
• 06924274910381: SY-VB(N)-1
• 6924274912255: SY-VB(N)-0
• 6924274912200: SY-IVB(N)-1
• 6924274912156: SY-IVB（N）-0
• 6924274912101: SY-IVB-1
• 6924274912057: SY-IVB-0
• 6924274912002: SY-IVA-1
• 6924274911951: SY-IVA-0
• 6924274911906: SY-IIIX(N)-1
• 6924274911852: SY-IIIB(Q)-0
• 6924274911807: SY-IIIB-2
• 6924274911753: SY-IIIB-1
• 6924274911708: SY-IIIB-0
• 6924274911654: SY-IIIA(N)-1
• 6924274911609: SY-IIIA(N)-0
• 6924274911555: SY-IIIA-2
• 6924274911500: SY-IIIA-1
• 6924274911456: SY-IIIA-0
• 6924274911401: SY-IIB(JN)-0
• 6924274911357: SY-IIB(N)-2
• 6924274911302: SY-IIB(N)-1
• 06924274910176: SY-IIB(N)-0
• 6924274911203: SY-IIB-2
• 6924274911159: SY-IIB-1
• 6924274911104: SY-IIB-0
• 6924274911050: SY-IIA(N)-2
• 6924274911005: SY-IIA(N)-1
• 06924274910114: SY-IIA(N)-0
• 6924274910909: SY-IIA-2
• 6924274910855: SY-IIA-1
• 6924274910800: SY-IIA-0
• 6924274910756: SY-IB-3
• 6924274910701: SY-IB-2
• 06924274910053: SY-IB-1
• 06924274910046: SY-IB-0
• 6924274910558: SY-IA(J)-0
• 6924274910503: SY-IA-2
• 6924274910459: SY-IA-1
• 6924274910404: SY-IA-0
• 16924274957161: ISEP1000
• 16924274958083: SY-IB-1