| Primary Device ID | 08033390117722 |
| NIH Device Record Key | 953d5480-42da-4a75-9517-c06bdfa70847 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Delta Cup |
| Version Model Number | 9055.60.111 |
| Catalog Number | 9055.60.111 |
| Company DUNS | 432066322 |
| Company Name | LIMACORPORATE SPA |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 08033390117722 [Primary] |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08033390117722]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-07-03 |
| Device Publish Date | 2019-06-25 |
| 08033390117722 | Neck Positioner for Press |
| 08033390117715 | Double Mobility Press |
| 08033390117692 | Head Pusher |
| 08033390062817 | Trial Liner #M for Dual Mobility Dia. 40 mm |
| 08033390062183 | Trial Mobile Liner Dia. 42 mm for Head Dia. 28 mm |
| 08033390059794 | Trial Mobile Liner Dia. 40 mm for Head Dia. 28 mm |
| 08033390059763 | Trial Liner #L for Dual Mobility Dia. 42 mm |
| 08033390071857 | Curved Impactor |
| 08033390058896 | Curved Impactor |
| 08033390058889 | Adapter Large for Curved Impactor |
| 08033390058858 | Adapter Medium for Curved Impactor |
| 08033390058469 | Adapter Small for Curved Impactor |