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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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ROCHESTER-PÉAN STILLE ARTERY FORCEPS — 1 UDI-DI variant, MDD

MD Atlas
Stille AB

Data from EUDAMED, last updated May 30, 2026

ROCHESTER-PÉAN STILLE ARTERY FORCEPS

B-07332339203030

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: Stille AB

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: B-07332339203030
Device name: ROCHESTER-PÉAN STILLE ARTERY FORCEPS
Device model: 103-10202-181
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Apr 26, 2023

Manufacturer & authorised representative

Manufacturer

Name: Stille AB
SRN: SE-MF-000001228
Country: Sweden
Email: katalin.daroczy@stille.se
Phone: +46 72 402 34 14

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01GYY8BATGYGE88R7B2H8EFJTY

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

ROCHESTER-PÉAN STILLE ARTERY FORCEPS07332339203030