Obstetrical Kit

GUDID 00616784490137

DYNAREX CORPORATION

Obstetrical/gynaecological surgical procedure kit, medicated

• Primary Device ID: 00616784490137
• NIH Device Record Key: 7091c45e-3729-487c-9077-bcba455d0bbe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Obstetrical Kit
• Version Model Number: 4901
• Company DUNS: 008124539
• Company Name: DYNAREX 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00616784490120 [Primary]
GS1	00616784490137 [Package]; Contains: 00616784490120; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• KNA: Instrument, Manual, Specialized Obstetric-Gynecologic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

On-Brand Devices [Obstetrical Kit]

• 00616784490236: 4902
• 00616784490137: 4901