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Allis Grasper Ø 5 mm x 310 mm

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref X0007002Model Senhance Surgical Instruments

by Asensus Surgical Italia S.r.l.

Identity

Trade Name
Allis Grasper Ø 5 mm x 310 mm EUDAMED
Senhance FDA UDI
Generic Name
Robotic surgical forceps, reusable FDA UDI
Device Name
Allis Grasper FDA UDI
Model / Reference
Senhance Surgical Instruments EUDAMED
X0007002 EUDAMEDFDA UDI
Description
Allis Grasper FDA UDI

Identifiers

Catalog Number
200-11026 FDA UDI
Primary DI / UDI-DI
00815440020002 EUDAMEDFDA UDI
Basic UDI-DI
081544002TD005UM EUDAMED
Direct Marketing DI
00815440020002 EUDAMED
510(k) Number
K171120 FDA UDI
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 EUDAMED
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Market of Registration
Croatia 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 310 Millimeter FDA UDI
Outer Diameter — 5 Millimeter FDA UDI

Allis Grasper Ø 5 mm x 310 mm by Asensus Surgical Italia S.r.l. — 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

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Manufacturer

EUDAMED SRN
IT-MF-000007964

Sources (2)

  • EUDAMED cb386183-95a3-4ea8-9883-ad60f3b8bb6d 61 fields · synced Jun 18, 2026
  • FDA UDI 404d1b76-58a7-479e-8509-5436dbe3612e 36 fields · synced May 30, 2026