Primary Device ID | 04026575329908 |
NIH Device Record Key | e747b7c0-2e62-4047-ae00-3df9bf93add0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vario-Cup System |
Version Model Number | 107-230/62 |
Company DUNS | 315675488 |
Company Name | WALDEMAR LINK GmbH & Co. KG |
Device Count | 1 |
DM Exempt | true |
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 | false |
Serial Number | true |
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 | 04026575329908 [Primary] |
KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-22 |
Device Publish Date | 2023-03-14 |
04026575395910 | Safety Ring, for Head Ø 22mm |
04026575352791 | Vario-Cup, ID22 OD43 |
04026575352784 | Vario-Cup, ID22 OD42 |
04026575352777 | Vario-Cup, ID22 OD41 |
04026575352760 | Vario-Cup, ID22 OD40 |
04026575352753 | Vario-Cup, ID22 OD39 |
04026575395903 | Safety Ring, UHMWPE, cementless |
04026575329939 | 107-230/65 |
04026575329922 | 107-230/64 |
04026575329915 | 107-230/63 |
04026575329908 | 107-230/62 |
04026575329892 | 107-230/61 |
04026575329885 | 107-230/60 |
04026575329878 | 107-230/59 |
04026575329861 | 107-230/58 |
04026575329854 | 107-230/57 |
04026575329847 | 107-230/56 |
04026575329830 | 107-230/55 |
04026575329823 | 107-230/54 |
04026575329816 | 107-230/53 |
04026575329809 | 107-230/52 |
04026575329793 | 107-230/51 |
04026575329786 | 107-230/50 |
04026575329779 | 107-230/49 |