| Primary Device ID | 00893398002271 |
| NIH Device Record Key | 077c88e4-0a33-48b4-9e23-fc19e6c06a5b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tissu-Trans MEGA |
| Version Model Number | Tissu-Trans MEGA 1500 |
| Catalog Number | 3-TT-MEGA 1500 |
| Company DUNS | 051437143 |
| Company Name | SHIPPERT MEDICAL TECHNOLOGIES, INC |
| 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 | false |
| 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 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00893398002271 [Primary] |
| MUU | System, Suction, Lipoplasty |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2020-05-06 |
| Device Publish Date | 2016-08-10 |
| 00893398002004 - DENVER SPLINT | 2023-05-08 |
| 00893398002011 - DENVER SPLINT | 2023-05-08 |
| 00893398002035 - DENVER SPLINT | 2023-05-08 |
| 00893398002042 - DENVER SPLINT | 2023-05-08 |
| 00893398002066 - DENVER SPLINT | 2023-05-08 |
| 00893398002103 - DENVER SPLINT | 2023-05-08 |
| 00893398002110 - DENVER SPLINT | 2023-05-08 |
| 00893398002127 - DENVER SPLINT | 2023-05-08 |