Primary Device ID | 00192896009233 |
NIH Device Record Key | 9bd9b518-1273-4dde-9ca0-ac9b79e4057b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FORCEPS CORD |
Version Model Number | A827F |
Catalog Number | A827F |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896009233 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896009233]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896009233]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896009233]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-17 |
Device Publish Date | 2018-08-15 |
00192896009233 | FORCEPS CORD |
00192896009226 | FORCEPS CORD |