Primary Device ID | B09929013030 |
NIH Device Record Key | 0fac9356-afd6-4a8c-b1f2-bfbd4ef2fb2a |
Commercial Distribution Discontinuation | 2018-06-22 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | POWER CUT PREPARATION SCISSORS |
Version Model Number | 2901-303 |
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 |
Length | 360 Millimeter |
Device Size Text, specify | 0 |
Length | 360 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B09929013030 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B09929013030]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09929013030]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 8 |
Public Version Date | 2018-12-21 |
Device Publish Date | 2016-08-19 |
B09929013030 | POWER CUT PREPARATION SCISSORS CURVED DOUBLE-ACTION JAW |
00192896115088 | Power Cut Preparation Scissors Curved Double Action Jaw Insert For 5 Millimeter Diameter Tube Sh |