Primary Device ID | 04059082014494 |
NIH Device Record Key | 1b853bc6-66d9-4a03-ba6b-3f058761ad8d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Needle holder |
Version Model Number | 392 992 001 |
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 | 04059082014494 [Primary] |
GCJ | Laparoscope, general & plastic surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
[04059082014494]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-12 |
04059082025247 | 394 560 049 |
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04059082014500 | 392 992 011 |
04059082014494 | 392 992 001 |