| Primary Device ID | 20844685003871 |
| NIH Device Record Key | 6100a9ed-fe82-48c3-9375-2e1692ed3832 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MST/Packard .7mm strt p tp Dwy 30º |
| Version Model Number | PT-32430-B |
| Catalog Number | PT-32430-B |
| Company DUNS | 097824130 |
| Company Name | MICROSURGICAL TECHNOLOGY, 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 | false |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20844685003871 [Primary] |
| HQC | Unit, Phacofragmentation |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20844685003871]
Radiation Sterilization;Moist Heat or Steam Sterilization
[20844685003871]
Radiation Sterilization;Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-11-23 |
| 00844685008391 - Snyder Ruler | 2024-07-15 |
| 00844685009442 - Accutome Surgical | 2024-07-15 Adson Bipolar Forceps |
| 00844685009459 - Accutome Surgical | 2024-07-15 McPherson Bipolar Forceps |
| 00844685009466 - Accutome Surgical | 2024-07-15 McPherson Bipolar Forceps |
| 00844685009480 - Accutome Surgical | 2024-07-15 Wide Handle Utrata 0.12 |
| 00844685010707 - Accutome Surgical | 2024-07-15 Utrata Capsulorhexis Forceps |
| 00844685010714 - Accutome Surgical | 2024-07-15 Utrata Capsulorhexis Forceps |
| 00844685010721 - Accutome Surgical | 2024-07-15 Utrata Capsulorhexis Forceps |