Primary Device ID | B0992800405L0 |
NIH Device Record Key | fdfaebe5-27e7-490c-abe3-5d8db2036f74 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HEARTLINE KNOT PUSHER FORCEPS |
Version Model Number | 2800-405L |
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 |
Length | 29 Centimeter |
Length | 29 Centimeter |
Length | 29 Centimeter |
Length | 29 Centimeter |
Length | 29 Centimeter |
Length | 29 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896010895 [Primary] |
HIBCC | B0992800405L0 [Previous] |
GCJ | Laparoscope, General & Plastic Surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B0992800405L0]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B0992800405L0]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B0992800405L0]
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 |
B0992800405L0 | HEARTLINE KNOT PUSHER FORCEPS HOOK & WEDGE SQUEEZE HANDLE |
B0992800405S0 | HEARTLINE KNOT PUSHER FORCEPS HOOK & WEDGE SQUEEZE HANDLE |
B09928004050 | HEARTLINE KNOT PUSHER FORCEPS HOOK & WEDGE SQUEEZE HANDLE |