Primary Device ID | 00889024145054 |
NIH Device Record Key | a931f083-5663-464a-9530-a805c9e3444e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ZCA® Longevity® |
Version Model Number | 8065-550-22 |
Company DUNS | 056038268 |
Company Name | Zimmer, Inc. |
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 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 22 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024145054 [Primary] |
JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-24 |