Primary Device ID | 04712771504781 |
NIH Device Record Key | 91e2f64f-755b-4159-947f-8028159bb7c0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ti Cancellous Screw |
Version Model Number | 5206-1060 |
Catalog Number | 5206-1060 |
Company DUNS | 656700556 |
Company Name | UNITED ORTHOPEDIC CORP. |
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 |
Phone | +886229294567 |
service@uoc.com.tw |
Device Size Text, specify | 0 |
Length | 60 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04712771504781 [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 | 4 |
Public Version Date | 2018-08-07 |
Device Publish Date | 2015-10-24 |
04712771504781 | Ti Cancellous Screw, Ø6.5 x 60mm |
04712771504774 | Ti Cancellous Screw, Ø6.5 x 55mm |
04712771504767 | Ti Cancellous Screw, Ø6.5 x 50mm |
04712771504750 | Ti Cancellous Screw, Ø6.5 x 45mm |
04712771504743 | Ti Cancellous Screw, Ø6.5 x 40mm |
04712771504736 | Ti Cancellous Screw, Ø6.5 x 35mm |
04712771504729 | Ti Cancellous Screw, Ø6.5 x 30mm |
04712771504712 | Ti Cancellous Screw, Ø6.5 x 25mm |
04712771504705 | Ti Cancellous Screw, Ø6.5 x20mm |
04712771504699 | Ti Cancellous Screw, Ø6.5 x 15mm |