Primary Device ID | 04260277177775 |
NIH Device Record Key | 0c7ced2a-f76b-4b97-abbc-7239a9bc72b6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | icotec Instrument Cement Cannula |
Version Model Number | 10002119 |
Catalog Number | 42-420 |
Company DUNS | 320405061 |
Company Name | Möller Medical GmbH |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04260277177768 [Primary] |
GS1 | 04260277177775 [Package] Contains: 04260277177768 Package: 42-421 [10 Units] In Commercial Distribution |
KIH | Dispenser, Cement |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-11-02 |
Device Publish Date | 2020-10-23 |
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