Primary Device ID | B09920941010 |
NIH Device Record Key | c58ddd5a-99d7-421a-8d25-5c02e0fd44a5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MICTEC INJECTION CANNULA |
Version Model Number | 20941-01 |
Company DUNS | 040729840 |
Company Name | SONTEC INSTRUMENTS, INC. |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 |
Phone | 800-821-7496 |
info@sontecinstruments.com | |
Phone | 800-821-7496 |
info@sontecinstruments.com | |
Phone | 800-821-7496 |
info@sontecinstruments.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896008731 [Primary] |
HIBCC | B09920941010 [Previous] |
HET | Laparoscope, Gynecologic (And Accessories) |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B09920941010]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09920941010]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09920941010]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-24 |
Device Publish Date | 2018-08-24 |
00192896008748 | MICTEC INJECTION CANNULA CURVED WITH GREAT LUER CONNECTION G18 |
B09920941010 | MICTEC INJECTION CANNULA CURVED SMALL LUER LOCK G22 |