| Primary Device ID | 00855204008006 |
| NIH Device Record Key | 0828d8e9-aa06-4564-8f1f-826ed21deda1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TPAK |
| Version Model Number | TM-303 |
| Catalog Number | TM-303 |
| Company DUNS | 078589992 |
| Company Name | TYTEK MEDICAL INC. |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | true |
| 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 | 00855204008006 [Primary] |
| GAA | Needle, Aspiration And Injection, Disposable |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-10-11 |
| Device Publish Date | 2019-10-03 |
| 00855204008051 | Tension Pneumothorax Decompression Needle: 10 gauge x 3.25" |
| 00855204008006 | Tension Pneumothorax Decompression Needle: 14 gauge x 3.25" |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TPAK 97740069 not registered Live/Pending |
Fluke Corporation 2023-01-03 |
![]() TPAK 87259271 not registered Live/Pending |
UNIT SOLUTIONS, INC. 2016-12-06 |
![]() TPAK 75586181 2318600 Dead/Cancelled |
Quick Pak, Inc. 1998-11-10 |