Primary Device ID | 00841439113424 |
NIH Device Record Key | a75085be-a810-4d33-9d47-9ae213be2815 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lok-Bar™ |
Version Model Number | MTVR1000 |
Catalog Number | MTVR1000 |
Company DUNS | 103977526 |
Company Name | MEDTEC, INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841439113424 [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 | 2021-06-14 |
Device Publish Date | 2021-06-05 |
00841439107591 | Reusable non-sterile MR T-Pin lok-bar |
00841439107492 | Lok-Bar™ (2-Pin) |
00841439107485 | Lok-Bar™ (3-Pin) |
00841439105085 | Transverse (50cm) |
00841439113424 | 50cm, Flat |