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Atraumatic Single Action Grasper Ø 3 mm x 280 mm
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref X0007203Model Senhance Surgical Instruments
Identity
- Trade Name
- Atraumatic Single Action Grasper Ø 3 mm x 280 mm EUDAMEDSenhance FDA UDI
- Generic Name
- Robotic surgical forceps, reusable FDA UDI
- Device Name
- Atraumatic Single Action Grasper FDA UDI
- Model / Reference
- Senhance Surgical Instruments EUDAMEDX0007203 EUDAMEDFDA UDI
- Description
- Atraumatic Single Action Grasper FDA UDI
Identifiers
- Catalog Number
- 200-11010 FDA UDI
- Primary DI / UDI-DI
- 00815440020620 EUDAMEDFDA UDI
- Basic UDI-DI
- 081544002TD005UM EUDAMED
- Direct Marketing DI
- 00815440020620 EUDAMED
- FDA Product Code
- NAY FDA UDI
- EMDN Code
- L1399 ROBOTIC SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Robotic surgical forceps, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 280 Millimeter FDA UDIOuter Diameter — 3 Millimeter FDA UDI
Category: Robotic surgical forceps, reusable
Atraumatic Single Action Grasper Ø 3 mm x 280 mm by Asensus Surgical Italia S.r.l. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
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Also classified as Robotic surgical forceps, reusable.
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- EndoWrist — Intuitive Surgical, Inc. · Class II
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 | 081544002TD005UM | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Asensus Surgical Italia S.r.l.
- EUDAMED SRN
- IT-MF-000007964
Sources (2)
- EUDAMED 2ef5624e-68e3-40c5-a0f1-7f294ce8ecf1 61 fields · synced Jul 18, 2026
- FDA UDI 84cf9bd3-c780-45f4-88a1-62dc9e4218b4 35 fields · synced May 30, 2026