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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Adapter, Allis Grasper Ø 5 mm x 240 mm — 80 UDI-DI variants, MDR

MD Atlas
Asensus Surgical Italia S.r.l.

Data from EUDAMED, last updated May 30, 2026

Adapter, Allis Grasper Ø 5 mm x 240 mm

081544002TD006UP

80 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Asensus Surgical Italia S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 081544002TD006UP
Device name: Adapter, Allis Grasper Ø 5 mm x 240 mm
Device model: Senhance Adapters
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 1, 2022

Manufacturer & authorised representative

Manufacturer

Name: Asensus Surgical Italia S.r.l.
SRN: IT-MF-000007964
Country: Italy
Email: asensus.italia@asensus.com
Phone: +39 0266111810

Variants by status

UDI-DI variants

80 UDI-DI variants

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Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

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