| Primary Device ID | 10381780490586 |
| NIH Device Record Key | e3359612-371d-49b3-8aa1-dbcec380b0f4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Integra® MicroFrance® |
| Version Model Number | MCOS10LP |
| Catalog Number | MCOS10LP |
| Company DUNS | 081277700 |
| Company Name | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
| 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 | true |
| 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)654-2873 |
| custsvcnj@integralife.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10381780490586 [Primary] |
| GEI | Electrosurgical, cutting & coagulation & accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10381780490586]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-02-05 |
| Device Publish Date | 2018-09-14 |
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