| Primary Device ID | 00844685002153 |
| NIH Device Record Key | 8a934fb4-68f3-4b74-b3c3-3b2e7afdf859 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Handle for Intertip Stainless I/A System |
| Version Model Number | IH-90200 |
| Catalog Number | IH-90200 |
| Company DUNS | 097824130 |
| Company Name | MICROSURGICAL TECHNOLOGY, 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 00844685002153 [Primary] |
| HMX | Cannula, Ophthalmic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00844685002153]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-07 |
| Device Publish Date | 2018-09-16 |
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