Primary Device ID | 00889024644151 |
NIH Device Record Key | 1dab8fbd-dc0c-4c2f-811b-c6b5f07dc666 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | APR® |
Version Model Number | 4338-32-067 |
Catalog Number | 4338-32-067 |
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 | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Lumen/Inner Diameter | 32 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024644151 [Primary] |
MEH | Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-03-07 |
Device Publish Date | 2022-02-25 |