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Needle Holder Left Ø 5 mm x 240 mm

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref Х0007022Model Senhance Surgical Instruments

by Asensus Surgical Italia S.r.l.

Identity

Trade Name
Needle Holder Left Ø 5 mm x 240 mm EUDAMED
Senhance FDA UDI
Generic Name
Robotic surgical forceps, reusable FDA UDI
Device Name
Needle Holder Left FDA UDI
Model / Reference
Senhance Surgical Instruments EUDAMED
Х0007022 EUDAMED
X0007022 FDA UDI
Description
Needle Holder Left FDA UDI

Identifiers

Catalog Number
200-11094 FDA UDI
Primary DI / UDI-DI
00815440021221 EUDAMEDFDA UDI
Basic UDI-DI
081544002TD005UM EUDAMED
Direct Marketing DI
00815440021221 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 EUDAMED
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Market of Registration
France 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 — 240 Millimeter FDA UDI
Outer Diameter — 5 Millimeter FDA UDI

Category: Robotic surgical forceps, reusable

Needle Holder Left Ø 5 mm x 240 mm by Asensus Surgical Italia S.r.l. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Robotic surgical forceps, reusable.

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 65c06587-e12d-443c-ad0a-15c49c1d8e4c 61 fields · synced Jul 9, 2026
  • FDA UDI 07b162e4-450b-42a3-972f-c231077cafab 35 fields · synced May 30, 2026