Primary Device ID | 00192896117044 |
NIH Device Record Key | 8d9fa0e0-4609-4d9e-ba96-5f88f4784b94 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sternal Internal Mammary Artery Retractor Blade |
Version Model Number | 2605-4502 |
Catalog Number | 2605-4502 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896117044 [Primary] |
GAD | RETRACTOR |
Steralize Prior To Use | true |
Device Is Sterile | false |
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Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-02 |
Device Publish Date | 2024-03-25 |
00192896117051 | Sternal Internal Mammary Artery Retractor Blade 25 Millimeter Titanium |
00192896117044 | Sternal Internal Mammary Artery Retractor Blade 20 Millimeter Titanium |