Primary Device ID | 00385640001724 |
NIH Device Record Key | 8906b09c-4ac0-49da-99a5-cb1cfb4f1189 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | VT-0903-01 |
Company DUNS | 965484699 |
Company Name | SUMMIT MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00385640001724 [Primary] |
GS1 | 10385640001721 [Package] Package: Box [6 Units] In Commercial Distribution |
GS1 | 20385640001728 [Package] Package: Box [50 Units] In Commercial Distribution |
ETD | Tube, Tympanostomy |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-12 |
00385640087674 - INSTRUSAFE | 2025-07-31 |
00385640087681 - INSTRUSAFE | 2025-07-31 |
00385640087698 - INSTRUSAFE | 2025-07-31 |
00385640087704 - INSTRUSAFE | 2025-07-31 |
00385640087711 - INSTRUSAFE | 2025-07-31 |
10385640086803 - SUMMIT MEDICAL | 2025-07-25 |
00385640087643 - INSTRUSAFE | 2025-07-24 |
00385640087650 - INSTRUSAFE | 2025-07-24 |