Primary Device ID | 00850077007118 |
NIH Device Record Key | c2297f0c-3433-41c6-a98f-dd56d1dce852 |
Commercial Distribution Discontinuation | 2016-12-05 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Husetis Medical Flexi-Holder |
Version Model Number | FH410-GE |
Company DUNS | 001188390 |
Company Name | HUESTIS MACHINE CORPORATION |
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 | false |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850077007118 [Primary] |
IXA | Cassette, Radiographic Film |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-11-01 |
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