Primary Device ID | 00192896093690 |
NIH Device Record Key | bb45ee03-9aef-4745-b7f0-e8a39644ec29 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RING CURETTE |
Version Model Number | 1271-148 |
Catalog Number | 1271-148 |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com |
Length | 9 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896093690 [Primary] |
HTF | CURETTE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896093690]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-05-07 |
Device Publish Date | 2019-03-07 |
00192896093690 | RING CURETTE ANGLED TIP ARTHROSCOPIC HANDLE |
00192896120105 | Ring Curette Sharp |
00192896120099 | Ring Curette Sharp |
00192896120082 | Ring Curette Sharp |
00192896120075 | Ring Curette Sharp |
00192896120068 | Ring Curette Sharp |
00192896120051 | Ring Curette Sharp |
00192896120044 | Ring Curette Sharp |
00192896120037 | Ring Curette Sharp |
00192896120020 | Ring Curette Blunt |
00192896120013 | Ring Curette Blunt |
00192896120006 | Ring Curette Blunt |
00192896119994 | Ring Curette Blunt |
00192896119987 | Ring Curette Blunt |
00192896119970 | Ring Curette Blunt |
00192896119963 | Ring Curette Blunt |
00192896119956 | Ring Curette Blunt |