Identity
- Trade Name
- Mara FDA UDI
- Generic Name
- Water vapour endometrial-ablation applicator FDA UDI
- Device Name
- Mara Water Vapor Probe Kit FDA UDI
- Model / Reference
- DDK-16-050 FDA UDI
- Description
- Mara Water Vapor Probe Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888937026887 FDA UDI
- PMA Number
- P160047 FDA UDI
- FDA Product Code
- MNB FDA UDI
- GMDN Term
- Water vapour endometrial-ablation applicator FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- 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
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
Category: Water vapour endometrial-ablation applicator
Mara by CooperSurgical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Water vapour endometrial-ablation applicator.
- Mara Water Vapor Probe Kit — AEGEA MEDICAL INC. · Class III
Cleared under the same submission
P160047 also covers:
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
- CooperSurgical, Inc.
Sources (1)
- FDA UDI a9c47fbf-1952-4f84-9f98-09c40ddee402 34 fields · synced Jun 9, 2026