Primary Device ID | 00841439106433 |
NIH Device Record Key | 6b67d10e-3229-453a-870b-8b75b46932b9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Grid Extension |
Version Model Number | MTIL6663 |
Catalog Number | MTIL6663 |
Company DUNS | 103977526 |
Company Name | MEDTEC, INC. |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 |
Length | 55.3 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841439106433 [Primary] |
IXQ | Table, radiographic, stationary top |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-05-30 |
Device Publish Date | 2017-08-02 |
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