Identity
- Trade Name
- Endoform Myriad FDA UDI
- Generic Name
- Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial FDA UDI
- Device Name
- Myriad is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired. FDA UDI
- Model / Reference
- MR03LG0505 FDA UDI
- Description
- Myriad is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired. FDA UDI
Identifiers
- Catalog Number
- SR03LG0505US FDA UDI
- Primary DI / UDI-DI
- 09421905067300 FDA UDI
- FDA Product Code
- FTL FDA UDIKGN FDA UDI
- GMDN Term
- Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Endoform Myriad by Aroa Biosurgery — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
K171231 also covers:
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
- Myriad Matrix™ Soft Tissue Bioscaffold — Aroa Biosurgery
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aroa Biosurgery
Sources (1)
- FDA UDI 2e7bc2c0-087d-4741-b0cf-58ba9c4efc53 39 fields · synced May 30, 2026