Primary Device ID | 00192896110984 |
NIH Device Record Key | a4f3ef0c-a7b5-43a3-b1fc-b1a25e6de859 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Egress Cannula |
Version Model Number | SC94-0322 |
Company DUNS | 040729840 |
Company Name | SONTEC INSTRUMENTS, 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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com |
Length | 12 Inch |
Device Size Text, specify | 0 |
Length | 12 Inch |
Device Size Text, specify | 0 |
Length | 12 Inch |
Device Size Text, specify | 0 |
Length | 12 Inch |
Device Size Text, specify | 0 |
Length | 12 Inch |
Device Size Text, specify | 0 |
Length | 12 Inch |
Device Size Text, specify | 0 |
Length | 12 Inch |
Device Size Text, specify | 0 |
Length | 12 Inch |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896110984 [Primary] |
GEA | CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896110984]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896110984]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896110984]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896110984]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896110984]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896110984]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896110984]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896110984]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-01 |
Device Publish Date | 2021-08-24 |
00192896087842 | EGRESS CANNULA WITH CONICAL OBTURATOR |
00192896087835 | EGRESS CANNULA WITH CONICAL OBTURATOR |
00192896087828 | EGRESS CANNULA WITH CONICAL OBTURATOR |
00192896087811 | EGRESS CANNULA WITH CONICAL OBTURATOR |
00192896087804 | EGRESS CANNULA WITH CONICAL OBTURATOR |
00192896070608 | EGRESS CANNULA WITH CONICAL OBTURATOR |
00192896070592 | EGRESS CANNULA WITH CONICAL OBTURATOR |
00192896070585 | EGRESS CANNULA WITH CONICAL OBTURATOR |
00192896100428 | EGRESS CANNULA WITH CONICAL OBTURATOR |
00192896104730 | Egress Cannula With Conical Obturator 8.1 Millimeter Inner Diameter |
00192896110830 | Egress Cannula With Conical Obturator 7.1 Millimeter Inner Diameter |
00192896110984 | Egress Cannula With Conical Obturator |
00192896110977 | Egress Cannula With Conical Obturator |
00192896115552 | Egress Cannula With Conical Obturator |