| Primary Device ID | 04059082026367 |
| NIH Device Record Key | 4c133f0c-7246-4bb4-96f2-4e16be59ce41 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Biopsy forceps |
| Version Model Number | 395 400 133 |
| Company DUNS | 507185952 |
| Company Name | SOPRO-COMEG 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04059082026367 [Primary] |
| HRX | ARTHROSCOPE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04059082026367]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-12 |
| 04059082026374 | 395 400 134 |
| 04059082026367 | 395 400 133 |
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