Primary Device ID | 00385640048798 |
NIH Device Record Key | 8cf81e37-6bfb-4769-b911-715276c23429 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SUMMIT MEDICAL |
Version Model Number | 3-C-1H1-12X10 |
Company DUNS | 965484699 |
Company Name | SUMMIT 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 | 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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00385640048798 [Primary] |
GEA | Cannula, Surgical, General & Plastic Surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00385640048798]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-27 |
Device Publish Date | 2019-11-19 |
00385640048774 | 3-C-T60-4H-4X25 |
00385640048767 | 3-C-GAN-18X15 |
00385640048750 | 3-C-MH-12X35 |
00385640048804 | 3-C-T60-BB-4X25 |
00385640048798 | 3-C-1H1-12X10 |
00385640049313 | 3-C-T60-1HV-3X15 |
00385640049344 | 3-C-MAN-12X10 |
00385640049337 | 3-C-T60-1H2-4X15 |
00385640049320 | 3-C-VDS-12X23 |
00385640049412 | 3-C-1H2-12X10 |
00385640049405 | 3-C-1H2-17X8 |
00385640049399 | 3-C-T60-1H2-4X25 |
00385640049498 | 3-C-T60-1H1-3X23 |
00385640049474 | 3-H-BA-MC-6X45 |
00385640049467 | 3-H-BA-MC-5X45 |