Resolve Matrix™ Biologic Membrane RMAD612
GUDID 00812337020497
DSM BIOMEDICAL, INC.
Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing Collagen wound matrix dressing| Primary Device ID | 00812337020497 |
| NIH Device Record Key | 88e0961c-3937-458f-9f58-2af2a022db05 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Resolve Matrix™ Biologic Membrane |
| Version Model Number | 30052-23 |
| Catalog Number | RMAD612 |
| Company DUNS | 131107757 |
| Company Name | DSM BIOMEDICAL, INC. |
| 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 | 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 |
Customer Support Contacts
Device Dimensions
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
| Length | 6 Centimeter |
| Width | 12 Centimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812337020497 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K112888
FDA Product Code
| KGN | Dressing, Wound, Collagen |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-03-01 |
| Device Publish Date | 2023-02-21 |
On-Brand Devices [Resolve Matrix™ Biologic Membrane]
| 00812337020534 | 30052-25 |
| 00812337020503 | 30052-24 |
| 00812337020497 | 30052-23 |
| 00812337020480 | 30052-22 |
| 00812337020473 | 30052-21 |
| 00812337020596 | Resolve Matrix™ 3 cm x 4 cm |
| 00812337020589 | Resolve Matrix™ 2 cm x 3 cm |
| 00812337020572 | Resolve Matrix™ 6 cm x 8 cm |
| 00812337020565 | Resolve Matrix™ 4 cm x 5 cm |
| 00812337020558 | Resolve Matrix™ 2 cm x 4 cm |
| 00812337020541 | Resolve Matrix™ 2 cm x 2 cm |
Trademark Results [Resolve Matrix]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RESOLVE MATRIX 97698534 not registered Live/Pending |
Parametrics Medical, LLC 2022-11-30 |
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