Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Blades — 38 UDI-DI variants, MDR (Black Forest Medical GmbH)

MD Atlas
Black Forest Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Blades

42504355PA0801Z4

38 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: Black Forest Medical GmbH

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Reusable

Legacy certificates

Certificate number: 1000297665
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: DQS Medizinprodukte GmbH (0297)
Validity: Jan 29, 2026 → Jul 5, 2028

Certificate number: 1000297641
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: DQS Medizinprodukte GmbH (0297)
Validity: Jan 29, 2026 → Mar 21, 2029

Identity & classification

Basic UDI-DI: 42504355PA0801Z4
Device name: Blades
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Mar 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: Black Forest Medical GmbH
SRN: DE-MF-000005752
Country: Germany
Email: info@blackforestmedical.com
Phone: +4976138422210

Variants by status

UDI-DI variants

38 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KKC2NZHNNS3JZFRYG9NXY2JF

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

3116-7504250435503591
3116-7104250435503553
3116-2104250435503171
3116-2204250435503188
3116-2304250435503195
3116-2404250435503201
3116-2504250435503218
3116-2604250435503225
3116-4104250435503317
3116-4204250435503324
3116-4304250435503331
3116-4404250435503348
3116-4504250435503355

1 2