Alloclassic® Zweymüller® 01.00121.040
GUDID 00889024481312
Zimmer GmbH
Press-fit hip femur prosthesis, modular| Primary Device ID | 00889024481312 |
| NIH Device Record Key | b94aeebe-0201-4f95-b674-3255da78b6a4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Alloclassic® Zweymüller® |
| Version Model Number | 01.00121.040 |
| Catalog Number | 01.00121.040 |
| Company DUNS | 488133448 |
| Company Name | Zimmer GmbH |
| 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 |
Customer Support Contacts
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
Device Dimensions
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024481312 [Primary] |
FDA Product Code
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-31 |
| Device Publish Date | 2017-07-28 |
On-Brand Devices [Alloclassic® Zweymüller®]
Trademark Results [Alloclassic]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ALLOCLASSIC 74582045 1938304 Live/Registered |
Zimmer GMBH 1994-10-04 |
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