ASSY, 220V PRESSURE PUMP

GUDID 00810040254017

GLOBAL SURGICAL CORPORATION

ENT cabinet

• Primary Device ID: 00810040254017
• NIH Device Record Key: c0432576-02a0-4559-a42a-c6b4025166f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASSY, 220V PRESSURE PUMP
• Version Model Number: 102-032-624
• Company DUNS: 824793335
• Company Name: GLOBAL SURGICAL CORPORATION
• 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: true
• Manufacturing Date: true
• Expiration Date: false
• 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	00810040254017 [Primary]

FDA Product Code

• ETF: Unit, Examining/Treatment, Ent

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: 2021-09-29
• Device Publish Date: 2021-09-21

Devices Manufactured by GLOBAL SURGICAL CORPORATION

• 00810040253836 - REP KIT FOR A-SERIES SCOPE: 2024-10-04
• 00810040254581 - LASER FILTER MODULE: 2024-10-04
• 00810040255113 - HD CAMERA, 1080P V2, A-SERIES: 2024-10-04
• 00810040255342 - CAMERA, 4K, USB POWER: 2024-10-04
• 00810040255397 - HD CAMERA, 1080P V2, FOR M725 SYS, INT'L: 2024-10-04
• 00810040255403 - LED LIGHT SOURCE, A-SERIES, V2: 2024-10-04
• 00810040255434 - A-SERIES SUPPORT ARM, HORIZONTAL, V2: 2024-10-04
• 00810040255441 - A-SERIES SUPPORT ARM, 45 DEGREE, V2: 2024-10-04