| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00616784420516 [Primary] |
| GS1 | 00616784420530 [Package] Package: [25 Units] In Commercial Distribution |
| NJZ | Extractor, Vein |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| 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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