| Primary Device ID | 04058749092103 |
| NIH Device Record Key | 467ce6be-52a4-47bc-85f4-c74d5aade7c8 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | TGB-4 |
| Catalog Number | TGB-4 |
| 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 | 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 | 800 334-5464 |
| info@fehlingsurgical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04058749092103 [Primary] |
| HAE | Rongeur, Manual |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04058749092103]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-07-24 |
| Device Publish Date | 2019-07-16 |
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