Primary Device ID | 00192896021280 |
NIH Device Record Key | 8542ec33-3051-4145-8a64-f2a3e9277ec7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BAINBRIDGE FORCEPS |
Version Model Number | 115-606 |
Catalog Number | 115-606 |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com |
Length | 7.25 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896021280 [Primary] |
HTD | FORCEPS |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896021280]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-08-21 |
Device Publish Date | 2018-09-14 |
00192896075658 | BAINBRIDGE FORCEPS DELICATE CURVED LONGITUDINAL CROSS SERRATED TIP |
00192896021280 | BAINBRIDGE FORCEPS DELICATE CURVED LONGITUDINAL SERRATIONS CROSS SERRATED TIP |
00192896021273 | BAINBRIDGE FORCEPS DELICATE STRAIGHT LONGITUDINAL SERRATIONS CROSS SERRATED TIP |
00192896021266 | BAINBRIDGE FORCEPS DELICATE CURVED LONGITUDINAL SERRATIONS CROSS SERRATED TIP |
00192896021259 | BAINBRIDGE FORCEPS LONG PRECISE RIGHT ANGLED LONGITUDINAL SERRATIONS TIP |
00192896021242 | BAINBRIDGE FORCEPS DELICATE STRAIGHT LONGITUDINAL SERRATIONS CROSS SERRATED TIP |
00192896116580 | Bainbridge Forceps Delicate Longitudinal Serrations Straight Cross Serrated Tip Quantum |