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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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Scanpost apol — 7 UDI-DI variants, MDR (APOL)

MD Atlas
APOL

Data from EUDAMED, last updated May 19, 2026

Scanpost apol

3665360SCANPOST9A

7 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: APOL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3665360SCANPOST9A
Device name: Scanpost apol
Device model: Scanpost
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: APOL
SRN: FR-MF-000001707
Country: France
Email: qualite@apol.fr
Phone: 0384522888

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KECADB9CE3WR7ERAW3DWXHGD

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

Scanpost bleu Ø1.4 L1636653600039304
Scanpost bleu Ø1.4 S1236653600039236
Scanpost jaune Ø1.6 L1636653600039540
Scanpost jaune Ø1.6 S1236653600039472
Scanpost rose Ø1.2 S1236653600039090
Scanpost vert Ø1.7 L1636653600039786
Scanpost vert Ø1.7 S1236653600039618