| Primary Device ID | 08033390059794 | 
| NIH Device Record Key | 6483bbed-aaa5-4bdf-8748-125b11e64496 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Delta Cup | 
| Version Model Number | 9055.65.040 | 
| Catalog Number | 9055.65.040 | 
| 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 Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 08033390059794 [Primary] | 
| MBL | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
Moist Heat or Steam Sterilization
[08033390059794]
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 |