Primary Device ID | 00880304203525 |
NIH Device Record Key | 283444a0-ad09-4874-a592-aff5bd64c15e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FREEDOM RINGLOC HIP SYSTEM |
Version Model Number | 11-107023 |
Catalog Number | 11-107023 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
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 | +1(800)348-9500 |
customerservice@zimmerbiomet.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304203525 [Primary] |
KWZ | Prosthesis, hip, constrained, cemented or uncemented, metal/polymer |
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 | 2015-10-24 |
00880304203839 | 11-107427 |
00880304203822 | 11-107426 |
00880304203815 | 11-107425 |
00880304203808 | 11-107424 |
00880304203785 | 11-107423 |
00880304203778 | 11-107327 |
00880304203761 | 11-107326 |
00880304203754 | 11-107325 |
00880304203747 | 11-107324 |
00880304203730 | 11-107323 |
00880304203723 | 11-107227 |
00880304203716 | 11-107226 |
00880304203709 | 11-107225 |
00880304203693 | 11-107224 |
00880304203686 | 11-107223 |
00880304203679 | 11-107222 |
00880304203570 | 11-107027 |
00880304203563 | 11-107026 |
00880304203556 | 11-107025 |
00880304203549 | 11-107024 |
00880304203525 | 11-107023 |
00880304203501 | 11-107022 |