Primary Device ID | 00887868356032 |
NIH Device Record Key | f261a542-15c4-42a3-b78e-7313cb2fb034 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | G7® OsseoTi® Acetabular Shell |
Version Model Number | 110010265 |
Catalog Number | 110010265 |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868356032 [Primary] |
OQG | Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-18 |
Device Publish Date | 2020-05-08 |
00887868356162 | 110010278 |
00887868356155 | 110010277 |
00887868356148 | 110010276 |
00887868356131 | 110010275 |
00887868356124 | 110010274 |
00887868356117 | 110010273 |
00887868356100 | 110010272 |
00887868356094 | 110010271 |
00887868356087 | 110010270 |
00887868356070 | 110010269 |
00887868356063 | 110010268 |
00887868356056 | 110010267 |
00887868356049 | 110010266 |
00887868356032 | 110010265 |
00887868356025 | 110010264 |
00887868356018 | 110010263 |
00887868356001 | 110010262 |
00887868355998 | 110010261 |
00887868355981 | 110010260 |
00887868355974 | 110010259 |
00887868355967 | 110010252 |
00887868355950 | 110010251 |
00887868355943 | 110010250 |
00887868355936 | 110010249 |
00887868355929 | 110010248 |
00887868355912 | 110010247 |
00887868355905 | 110010246 |
00887868355899 | 110010245 |
00887868355882 | 110010244 |
00887868355875 | 110010243 |
00887868355868 | 110010242 |
00887868355851 | 110010241 |
00887868355844 | 110010240 |