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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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PureHoney — 14 UDI-DI variants, MDR (Bfactory Health Products B.V.)

MD Atlas
Bfactory Health Products B.V.

Data from EUDAMED, last updated May 31, 2026

PureHoney

08717438PureHoneyST

14 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Bfactory Health Products B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 08717438PureHoneyST
Device name: PureHoney
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Dec 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: Bfactory Health Products B.V.
SRN: NL-MF-000021590
Country: Netherlands
Email: info@bfactory.nl
Phone: +310317769005

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KD55E64XM7KE58DTRN2YCD7D

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

1040008717438010229
1010008717438010007
1001008717438010632
1035008717438010656
1038008717438010717
1020008717438010045
1030408717438011011
1031808717438011080
1030208717438010618
1030508717438010397
1030708717438010441
1029508717438011578
1029708717438011585
1030008717438010175