Primary Device ID | 00192896101302 |
NIH Device Record Key | f2352eef-9348-4845-9f65-868a1d8fbd37 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NEONATAL MICRO VASCULAR FORCEPS |
Version Model Number | 2600-086 |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | 4.125 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896101302 [Primary] |
DWS | INSTRUMENTS, SURGICAL, CARDIOVASCULAR |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896101302]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-04-28 |
Device Publish Date | 2020-04-20 |
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00192896101302 | NEONATAL MICRO VASCULAR FORCEPS DOUBLE ANGLED TITANIUM |
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