Primary Device ID | B365501380 |
NIH Device Record Key | 8da11f9d-b1ac-4a55-b2f7-9444ab50c4a6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PinPoint Arch Support, Extended |
Version Model Number | 50-138 |
Company DUNS | 787178920 |
Company Name | Aktina Corp. |
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 | 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 |
---|---|
HIBCC | B365501380 [Primary] |
IYE | Accelerator, Linear, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-31 |
Device Publish Date | 2021-05-21 |
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