| Primary Device ID | 00857072005262 |
| NIH Device Record Key | 9986c6c5-f802-4ef0-9ce7-12a6e2af5799 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MiroDerm Fenestrated Plus |
| Version Model Number | BLM-200-03-0815 |
| 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 | 00857072005262 [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 |
| 00857072005262 | 8 x 15 cm Fenestrated Plus Biologic Wound Matrix |
| 00857072005255 | 7 x 10 cm Fenestrated Plus Biologic Wound Matrix |
| 00857072005248 | 8 x 8 cm Fenestrated Plus Biologic Wound Matrix |
| 00857072005231 | 5 x 5 cm Fenestrated Plus Biologic Wound Matrix |
| 00857072005224 | 3 x 7 cm Fenestrated Plus Biologic Wound Matrix |
| 00857072005217 | 4 x 4 cm Fenestrated Plus Biologic Wound Matrix |
| 00857072005200 | 3 x 3 cm Fenestrated Plus Biologic Wound Matrix |