Identity
- Trade Name
- MynxGrip Vascular Closure Device (5F) FDA UDI
- Generic Name
- Wound hydrogel dressing, non-antimicrobial FDA UDI
- Device Name
- MynxGrip Vascular Closure Device (5F) FDA UDI
- Model / Reference
- MX5021 FDA UDI
- Description
- MynxGrip Vascular Closure Device (5F) FDA UDI
Identifiers
- Catalog Number
- MX5021 FDA UDI
- Primary DI / UDI-DI
- M465MX50210 FDA UDI
- PMA Number
- P040044 FDA UDI
- FDA Product Code
- MGB FDA UDI
- GMDN Term
- Wound hydrogel dressing, non-antimicrobial FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Dimensions & Sizes
- Size
- Catheter Gauge — 5 French FDA UDI
MynxGrip Vascular Closure Device (5F) by Accessclosure, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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 III | Pending data |
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Manufacturer
- Manufacturer
- Accessclosure, Inc.
Sources (1)
- FDA UDI 8d9bb1b0-85be-4267-a4ef-71eef35a91ba 39 fields · synced Jun 8, 2026