Primary Device ID | B0992800205B0 |
NIH Device Record Key | 5027b9b5-8ec0-4ac5-bb90-6c1c76c76661 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HEARTLINE BLACK DIETHRICH POTTS SCISSORS |
Version Model Number | 2800-205B |
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 | 13.75 Inch |
Length | 13.75 Inch |
Length | 13.75 Inch |
Length | 13.75 Inch |
Length | 13.75 Inch |
Length | 13.75 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896006959 [Primary] |
HIBCC | B0992800205B0 [Previous] |
GCJ | Laparoscope, General & Plastic Surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B0992800205B0]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B0992800205B0]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B0992800205B0]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-12-21 |
Device Publish Date | 2018-08-22 |
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