Primary Device ID | 04712771502329 |
NIH Device Record Key | 3e64ec77-d07b-4808-805a-c399383b5be2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | United Hip System, U-Motion II HA Cup, Cluster-Hol |
Version Model Number | 1306-1054 |
Catalog Number | 1306-1054 |
Company DUNS | 656700556 |
Company Name | UNITED ORTHOPEDIC CORP. |
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 |
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04712771502442 | U-Motion II HA Cup, Ø78mm |
04712771502435 | U-Motion II HA Cup, Ø76mm |
04712771502428 | U-Motion II HA Cup, Ø74mm |
04712771502411 | U-Motion II HA Cup, Ø72mm |
04712771502404 | U-Motion II HA Cup, Ø70mm |
04712771502398 | U-Motion II HA Cup, Ø68mm |
04712771502381 | U-Motion II HA Cup, Ø66mm |
04712771502374 | U-Motion II HA Cup, Ø64mm |
04712771502367 | U-Motion II HA Cup, Ø62mm |
04712771502350 | U-Motion II HA Cup, Ø60mm |
04712771502343 | U-Motion II HA Cup, Ø58mm |
04712771502336 | U-Motion II HA Cup, Ø56mm |
04712771502329 | U-Motion II HA Cup, Ø54mm |
04712771502312 | U-Motion II HA Cup, Ø52mm |
04712771502305 | U-Motion II HA Cup, Ø50mm |
04712771502299 | U-Motion II HA Cup, Ø48mm |
04712771502282 | U-Motion II HA Cup, Ø46mm |
04712771502275 | U-Motion II HA Cup, Ø44mm |