Primary Device ID | B0992700968NS0 |
NIH Device Record Key | 2a71163a-cb2e-436c-96df-f1e6250239b2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BIPOLAR SCOVILLE GREENWOOD BAYONET FORCEPS |
Version Model Number | 2700-968NS |
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 | 7.5 Inch |
Length | 7.5 Inch |
Length | 7.5 Inch |
Length | 7.5 Inch |
Length | 7.5 Inch |
Length | 7.5 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896006621 [Primary] |
HIBCC | B0992700968NS0 [Previous] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B0992700968NS0]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B0992700968NS0]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B0992700968NS0]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-24 |
Device Publish Date | 2018-08-22 |
B0992700968NS0 | BIPOLAR SCOVILLE GREENWOOD BAYONET FORCEPS FLAT HANDLE NON-STICK |
B09927009450 | BIPOLAR SCOVILLE GREENWOOD BAYONET FORCEPS IRRIGATION INSULATION STRAIGHT |