Venom Extractor Kits

GUDID 00616784420516

Venom Extractor Kits

DYNAREX CORPORATION

Snake bite kit

• Primary Device ID: 00616784420516
• NIH Device Record Key: 5b3db5b0-c2b8-4e44-94df-03b00717375b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Venom Extractor Kits
• Version Model Number: 4205
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• 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: 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	00616784420516 [Primary]
GS1	00616784420530 [Package]; Package: [25 Units]; In Commercial Distribution

FDA Product Code

• NJZ: Extractor, Vein

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: 2020-11-10
• Device Publish Date: 2020-11-02

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