| Primary Device ID | 04048266143532 |
| NIH Device Record Key | 339ee7cb-24ed-4e09-915b-6dbe453d0cac |
| Commercial Distribution Discontinuation | 2021-12-13 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | MultiCup™ PE Inlay Standard |
| Version Model Number | Size 48 Head 32 |
| Catalog Number | HF74832 |
| 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 | 04048266143532 [Primary] |
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2021-12-14 |
| Device Publish Date | 2017-01-01 |
| 04048266143549 | MultiCup™ PE Inlay Standard, Size 48 Head 36 UHMWPE sterile |
| 04048266143532 | MultiCup™ PE Inlay Standard, Size 48 Head 32 UHMWPE sterile |
| 04048266143525 | MultiCup™ PE Inlay Standard, Size 41 Head 32 UHMWPE sterile |
| 04048266135797 | MultiCup™ PE Inlay Standard, Size 48 Head 28 UHMWPE sterile |
| 04048266135780 | MultiCup™ PE Inlay Standard, Size 41 Head 28 UHMWPE sterile |
| 04048266135773 | MultiCup™ PE Inlay Standard 37 for head 28 UHMWPE sterile |