Primary Device ID | 00841439106389 |
NIH Device Record Key | 178ae4c3-6b11-4ab6-a4b4-c17a61e9a960 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Patient Hand Grip |
Version Model Number | MTIL662502 |
Catalog Number | MTIL662502 |
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 | 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 |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Length | 7.91 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841439106389 [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 | 6 |
Public Version Date | 2020-03-31 |
Device Publish Date | 2017-08-02 |
00841439107287 | Patient Hand Grip - Left |
00841439106389 | For use with Universal Couchtop™ |
00841439106372 | For use with Universal Couchtop™ |