Primary Device ID | B09929012540 |
NIH Device Record Key | 80b25019-14a6-42e2-bb26-f1ede6722cff |
Commercial Distribution Discontinuation | 2018-06-22 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | DISSECTING FORCEPS INSERT |
Version Model Number | 2901-254 |
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 | B09929012540 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B09929012540]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B09929012540]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 7 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-19 |
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