| Primary Device ID | 04058749000030 |
| NIH Device Record Key | 8846c355-f364-48a8-8fc1-2aa162adbfa3 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | MOA-3 |
| Catalog Number | MOA-3 |
| Company DUNS | 315028238 |
| Company Name | Fehling Instruments GmbH & Co. KG |
| 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 | 800 334-5464 |
| info@fehlingsurgical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04058749000030 [Primary] |
| DWZ | Device, Biopsy, Endomyocardial |
| 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 | 2017-06-23 |
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