Primary Device ID | B09920928010 |
NIH Device Record Key | efeeba2f-2323-43ed-b5ee-43412a37edea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MICASEPT BIOPSY / SCISSOR FORCEPS |
Version Model Number | 20928-01 |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896008670 [Primary] |
HIBCC | B09920928010 [Previous] |
GCJ | Laparoscope, General & Plastic Surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B09920928010]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09920928010]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09920928010]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-24 |
Device Publish Date | 2018-08-24 |
B09920934030 | MICASEPT CIRADUR PE-FORCEPS POINTED CURVED DOWN |
B09920928010 | MICASEPT CIRADUR METZENBAUM SCISSORS CURVED LEFT CURVED DOWN |