| Primary Device ID | 00857072005156 |
| NIH Device Record Key | 05580552-e2a0-46a5-bea6-71a72b2d6b6f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MiroDerm Fenestrated |
| Version Model Number | BLM-200-02-0815 |
| Company DUNS | 043611421 |
| Company Name | REPRISE BIOMEDICAL, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00857072005156 [Primary] |
| KGN | Dressing, Wound, Collagen |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-08 |
| Device Publish Date | 2020-09-30 |
| 00857072005309 | 2x2 cm Fenestrated Biologic Wound Matrix |
| 00857072005293 | 2x3 cm Fenestrated Biologic Wound Matrix |
| 00857072005170 | 4 x 4 cm Fenestrated Biologic Wound Matrix |
| 00857072005163 | 3 x 3 cm Fenestrated Biologic Wound Matrix |
| 00857072005156 | 8 x 15 cm Fenestrated Biologic Wound Matrix |
| 00857072005149 | 7 x 10 cm Fenestrated Biologic Wound Matrix |
| 00857072005132 | 8 x 8 cm Fenestrated Biologic Wound Matrix |
| 00857072005125 | 5 x 5 cm Fenestrated Biologic Wound Matrix |
| 00857072005118 | 3 x 7 cm Fenestrated Biologic Wound Matrix |