Primary Device ID | B09929012020 |
NIH Device Record Key | a6927936-a416-46e9-85ea-126e12a6f487 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MARYLAND GRASPING FORCEPS INSERT |
Version Model Number | 2901-202 |
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 |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Length | 210 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896007475 [Primary] |
HIBCC | B09929012020 [Previous] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B09929012020]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09929012020]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09929012020]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-05-08 |
Device Publish Date | 2018-08-22 |
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