Primary Device ID | 00861578000393 |
NIH Device Record Key | 1f4133f0-39a4-4a9e-b9bd-10c21fc58264 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | mi-probe |
Version Model Number | T900-011 |
Catalog Number | T900-015 |
Company DUNS | 009452895 |
Company Name | TRICE MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 844.643.9300 |
customerservice@tricemedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00861578000386 [Primary] |
GS1 | 00861578000393 [Package] Contains: 00861578000386 Package: box [5 Units] In Commercial Distribution |
HXB | Probe |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-05-11 |
Device Publish Date | 2018-04-10 |
00857356008026 - mi-eye 2 | 2023-11-17 MI-EYE 2 SYSTEM, MI-ULTRA, EN |
00857356008118 - mi-eye 2 | 2023-11-17 TRICE MI-EYE ANGLED NEEDLESCOPE, 120MM |
00857356008224 - mi-tablet 3 | 2023-11-17 mi-tablet 3 |
00857356008231 - mi-eye 3 | 2023-11-17 mi-eye 3 needlescope, 95mm |
00857356008248 - mi-eye 3 | 2023-11-17 mi-eye 3 angled scope, 120mm |
00857356008255 - mi-eye 3 | 2023-11-17 mi-eye 3 25 deg scope, 75mm with cannula |
00857356008262 - mi-eye 3 | 2023-11-17 mi-eye 3 scope, 95mm with cannula |
00857356008279 - mi-eye 3 | 2023-11-17 mi-eye 3 25° scope, 75mm with cannula |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MI-PROBE 87683042 5764532 Live/Registered |
Trice Medical, Inc. 2017-11-13 |