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235mm Maxi Grasper

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 101-47026

by Surgical Innovations Ltd.

Identity

Trade Name
235mm Maxi Grasper EUDAMED
Logic - Laparoscopic Instrument System FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, reusable FDA UDI
Device Name
235mm Maxi Grasper EUDAMEDFDA UDI
Model / Reference
101-47026 EUDAMEDFDA UDI
Description
235mm Maxi Grasper FDA UDI

Identifiers

Primary DI / UDI-DI
05051986006802 EUDAMEDFDA UDI
Basic UDI-DI
B-05051986006802 EUDAMED
510(k) Number
K111986 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
L1899 ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Endoscopic electrosurgical electrode, monopolar, reusable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Market of Registration
Ireland 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

Category: Electrical-only medical device connection cable, reusable

235mm Maxi Grasper by Surgical Innovations Ltd. — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
GB-MF-000012187
Authorised Representative
CS Life Sciences Europe Ltd IE-AR-000004113

Sources (2)

  • EUDAMED 8e159a25-a5a4-4d17-943e-79ef87033e61 61 fields · synced Jul 19, 2026
  • FDA UDI 6dd3289c-9e51-4951-b55d-7793d62532fe 34 fields · synced May 27, 2026