Primary Device ID | 00889024154292 |
NIH Device Record Key | 43669732-b1af-46eb-943f-26b4491d0287 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Continuum® |
Version Model Number | 00-8834-023-36 |
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 | 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 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Lumen/Inner Diameter | 36 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024154292 [Primary] |
LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
[00889024154292]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2016-08-31 |
00889024154889 | 00-8838-023-36 |
00889024154872 | 00-8838-023-32 |
00889024154865 | 00-8838-022-36 |
00889024154858 | 00-8838-022-32 |
00889024154612 | 00-8835-023-36 |
00889024154605 | 00-8835-023-32 |
00889024154599 | 00-8835-022-36 |
00889024154582 | 00-8835-022-32 |
00889024154292 | 00-8834-023-36 |
00889024154285 | 00-8834-022-36 |
00889024153998 | 00-8832-023-36 |
00889024153981 | 00-8832-023-32 |
00889024153974 | 00-8832-022-36 |
00889024153967 | 00-8832-022-32 |
00889024153523 | 00-8831-023-40 |
00889024153516 | 00-8831-023-36 |
00889024153509 | 00-8831-022-40 |
00889024153493 | 00-8831-022-36 |
00889024151192 | 00-8757-000-02 |
00889024151185 | 00-8757-000-01 |