Primary Device ID | 07630055242549 |
NIH Device Record Key | d0ca4522-24bf-44a3-b6c3-6ec3643baa5e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bimanual I/A CR23 |
Version Model Number | MBSCR23 |
Catalog Number | MBSCR23 |
Company DUNS | 487158263 |
Company Name | Medicel AG |
Device Count | 10 |
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 |
Phone | +41717271050 |
info@medicel.com | |
Phone | +41717271050 |
info@medicel.com | |
Phone | +41717271050 |
info@medicel.com | |
Phone | +41717271050 |
info@medicel.com | |
Phone | +41717271050 |
info@medicel.com | |
Phone | +41717271050 |
info@medicel.com | |
Phone | +41717271050 |
info@medicel.com | |
Phone | +41717271050 |
info@medicel.com | |
Phone | +41717271050 |
info@medicel.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07630055242549 [Unit of Use] |
GS1 | 07640123277779 [Primary] |
HMX | Cannula, Ophthalmic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-16 |
Device Publish Date | 2021-09-08 |
07630055242549 | The Irrigation-/Aspiration Handpieces are used to remove the opaque human lens during cataract s |
07630055243782 | The Irrigation-/Aspiration Handpieces are used to remove the opaque human lens during cataract s |