| Primary Device ID | 00889024304895 |
| NIH Device Record Key | 237bb6a0-bd84-4b0b-a96c-3a3ff795eed8 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 20-8000-020-15 |
| Catalog Number | 20-8000-020-15 |
| Company DUNS | 205670032 |
| Company Name | Orthosoft 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 |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | 1(800)-348-2759 |
| zimmer.consumerrelations@zimmer.com |
| 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 | 00889024304895 [Primary] |
| HAW | Neurological Stereotaxic Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
[00889024304895]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-12 |
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| 00887868557903 - ROSA® Shoulder | 2024-03-14 |
| 00887868557910 - ROSA® Shoulder | 2024-03-14 |
| 00887868558078 - ROSA® Shoulder | 2024-03-14 |
| 00887868558092 - ROSA® Shoulder | 2024-03-14 |