Primary Device ID | 00873263003190 |
NIH Device Record Key | 3685c403-1095-4c6b-ba79-3f9947b7ada7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WayPoint™ Implant Kit |
Version Model Number | 66-WP-IKS-00319 |
Catalog Number | 66-WP-IKS |
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 |
Storage Environment Humidity | Between 0 and 95 Percent (%) Relative Humidity |
Storage Environment Humidity | Between 0 and 95 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00873263003190 [Primary] |
HAW | Neurological stereotaxic Instrument |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00873263003190]
Ethylene Oxide
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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