Primary Device ID | 04048266167620 |
NIH Device Record Key | a4f86424-34f0-4901-ae58-860113a2e2d2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DuoMetaCun™ II Plate |
Version Model Number | 31 28 |
Catalog Number | FH07031S |
Company DUNS | 313267265 |
Company Name | Merete 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 | 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 | 04048266167620 [Primary] |
KTT | Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2023-05-05 |
Device Publish Date | 2018-08-14 |
04048266167637 | DuoMetaCun™ II Plate with Compression-Hole Size 33 28 TiAl6V4 ELI sterile |
04048266167620 | DuoMetaCun™ II Plate with Compression-Hole Size 31 28 TiAl6V4 ELI sterile |
04048266167576 | DuoMetaCun™ II Plate with Compression-Hole Size 33 25 TiAl6V4 ELI non-sterile |
04048266167569 | 31 25 |