Primary Device ID | 10840843106593 |
NIH Device Record Key | 9f0a3d0d-5893-4eb3-a3fe-a0aea768fb83 |
Commercial Distribution Discontinuation | 2016-06-14 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Surpass Acetabular system |
Version Model Number | SC2603-28MM +3.5 |
Company DUNS | 804792265 |
Company Name | Stelkast Incorporated |
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 | 10840843106593 [Primary] |
MRA | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2014-11-20 |
10840843106807 | SC2645-72 |
10840843106791 | SC2645-70 |
10840843106784 | SC2645-68 |
10840843106777 | SC2645-66 |
10840843106760 | SC2645-64 |
10840843106753 | SC2645-62 |
10840843106746 | SC2645-60 |
10840843106739 | SC2645-58 |
10840843106722 | SC2645-56 |
10840843106715 | SC2645-54 |
10840843106708 | SC2645-52 |
10840843106692 | SC2645-50 |
10840843106685 | SC2645-48 |
10840843106678 | SC2645-46 |
10840843106630 | SC2641-32MM -3.5 |
10840843106623 | SC2641-32MM +3.5 |
10840843106616 | SC2641-32MM +0 |
10840843106609 | SC2603-28MM -3.5 |
10840843106593 | SC2603-28MM +3.5 |
10840843106586 | SC2603-28MM +0 |