Primary Device ID | 00841439114919 |
NIH Device Record Key | 959442de-a45d-4fe9-b00e-a67865c0f778 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Headrest - Timo Size F |
Version Model Number | MTTIMO2F |
Catalog Number | MTTIMO2F |
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 |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841439114919 [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 | 2024-12-12 |
Device Publish Date | 2024-12-04 |
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