620-010-101

GUDID 07613327063189

Veress Needle

STRYKER CORPORATION

Spring-loaded pneumoperitoneum needle, reusable

• Primary Device ID: 07613327063189
• NIH Device Record Key: 1d0131b4-2fb2-4719-9f19-a172e7b5de70
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 0620010101
• Catalog Number: 620-010-101
• Company DUNS: 187502109
• Company Name: STRYKER CORPORATION
• 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: false
• Lot Batch: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(866)624-4422
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327063189 [Primary]

FDA Product Code

• HIG: INSUFFLATOR, HYSTEROSCOPIC

Sterilization

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

[07613327063189]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-23

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