| Primary Device ID | 00827002172708 |
| NIH Device Record Key | 567166e0-6a8f-4ee7-b3e4-da34e0e78bf0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Aspiracath |
| Version Model Number | G17270 |
| Catalog Number | J-ASP-092500 |
| Company DUNS | 042823948 |
| Company Name | COOK INCORPORATED |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(812)330-5494 |
| sharedservices@cookmedical.com |
| Special Storage Condition, Specify | Between 0 and 0 *Store in dark, dry, cool place. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00827002172708 [Primary] |
| HFC | ASPIRATOR, ENDOCERVICAL |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-11-04 |
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| 00827002560833 - COOK | 2024-05-23 Captura Serrated Jumbo Forcep - No Spike |
| 00827002214521 - COOK | 2024-04-03 GLO-TIP ERCP CATHETER |
| 00827002215009 - COOK | 2024-04-03 GLO-TIP ERCP CATHETER |
| 00827002217652 - COOK | 2024-04-03 CLASSIC ERCP CATHETER |
| 00827002218680 - COOK | 2024-04-03 HUIBREGTSE-KATON ERCP CATHETER |
| 00827002219656 - COOK | 2024-04-03 GLO-TIP ERCP CATHETER |