| Primary Device ID | 10873263003494 |
| NIH Device Record Key | 195a4ff8-3a0e-441b-bd82-6127eb9451e5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | microTargeting Insertion Tube |
| Version Model Number | 66-IT-AR4P-00349 |
| Catalog Number | 66-IT-AR4P |
| Company DUNS | 108179458 |
| Company Name | FHC, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 |
| Phone | +1(800)326-2905 |
| fhcinc@fh-co.com |
| Outer Diameter | 1.83 Millimeter |
| Outer Diameter | 1.83 Millimeter |
| Outer Diameter | 1.83 Millimeter |
| Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Handling Environment Humidity | Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00873263003497 [Primary] |
| GS1 | 10873263003494 [Package] Contains: 00873263003497 Package: PK/5 [5 Units] In Commercial Distribution |
| HAW | Neurological stereotaxic Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[10873263003494]
Ethylene Oxide;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 | 2016-09-17 |
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