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Aveta Wave+ Disposable Resecting Device, 3.9 mm
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 210-2005
Identity
- Trade Name
- Aveta Wave+ Disposable Resecting Device, 3.9 mm EUDAMEDFDA UDI
- Generic Name
- Tissue morcellation system handpiece, line-powered FDA UDI
- Device Name
- Aveta Wave+ Disposable Resecting Device, 3.9 mm EUDAMEDAveta Wave+ Disposable Resecting Device, 3.9 mm, for use with Aveta System FDA UDI
- Model / Reference
- 210-2005 EUDAMEDFDA UDI
- Description
- Aveta Wave+ Disposable Resecting Device, 3.9 mm, for use with Aveta System FDA UDI
Identifiers
- Catalog Number
- 210-2005 FDA UDI
- Primary DI / UDI-DI
- 00850006759590 EUDAMEDFDA UDI
- Basic UDI-DI
- 00850006759590DZ EUDAMED
- 510(k) Number
- K190372 FDA UDI
- FDA Product Code
- HIG FDA UDIHIH FDA UDI
- EMDN Code
- Z12080204 MORCELLATORS EUDAMED
- GMDN Term
- Tissue morcellation system handpiece, line-powered FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 884.1700 FDA UDI884.1690 FDA UDI
- Market of Registration
- Denmark EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Aveta Wave+ Disposable Resecting Device, 3.9 mm by Meditrina, Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 00850006759590DZ | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Meditrina, Inc.
- EUDAMED SRN
- US-MF-000033191
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (2)
- EUDAMED 56cd9b7e-f2d8-4796-849a-3b02fc7a1fc5 61 fields · synced Jul 16, 2026
- FDA UDI adfc77ad-6b2a-43bc-b63c-98dc258747dd 35 fields · synced May 30, 2026