Primary Device ID | 04059082019048 |
NIH Device Record Key | 3b855bbc-d63d-424e-b554-7e6de9c0d6bb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dissecting forceps |
Version Model Number | 393 510 133 |
Company DUNS | 507185952 |
Company Name | SOPRO-COMEG GmbH |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04059082019048 [Primary] |
GCJ | Laparoscope, general & plastic surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04059082019048]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-12 |
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04059082019048 | 393 510 133 |
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