Primary Device ID | 10852073002637 |
NIH Device Record Key | 7a87beab-8428-4e86-8d44-8419dc13c3f7 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | K-UMI |
Catalog Number | TMI6003 |
Company DUNS | 130814890 |
Company Name | C R I |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | (800) 556-0349 |
Sales@ThomasMedical.com |
Outer Diameter | 5 Millimeter |
Outer Diameter | 5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852073002630 [Primary] |
GS1 | 10852073002637 [Package] Contains: 00852073002630 Package: Box [12 Units] In Commercial Distribution |
LKF | Cannula, Manipulator/Injector, Uterine |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-07 |
Device Publish Date | 2016-10-10 |
10852073002361 - NA | 2020-07-02 Round Loop, Loop Size: 20mm x 13mm |
10852073002378 - NA | 2020-07-02 Round Loop, Loop Size: 20mm x 15mm |
10852073002316 - NA | 2020-06-29 Round Loop, Loop Size: 15mm x 15mm |
10852073002484 - NA | 2020-06-29 Round Loop, Loop Size: 15mm x 10mm |
00852073002814 - NA | 2020-01-21 Balloon catheter with an insertion sheath for hysterosalpingography and sonohysterography for use with saline or water-based con |
10852073002231 - NA | 2019-05-27 Square Loop, Loop Size: 10mm x 4mm |
10852073002248 - NA | 2019-05-27 Round Loop, Loop Size: 5mm x 5mm |
10852073002255 - NA | 2019-05-27 Round Loop, Loop Size: 10mm x 5mm |