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.

Distal Augmentation Trial — 23 UDI-DI variants, MDR (DePuy Ireland UC)

MD Atlas
DePuy Ireland UC

Data from EUDAMED, last updated May 24, 2026

Distal Augmentation Trial

0603295a001628H

23 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: DePuy Ireland UC

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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0603295a001628H
Device name: Distal Augmentation Trial
Device model: PFC SIGMA Distal Augmentation Trial
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: DePuy Ireland UC
SRN: IE-MF-000007377
Country: Ireland
Email: EUDAMED_Enquiries@its.jnj.com
Phone: +353 (0)214914000

Variants by status

UDI-DI variants

23 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

basicUdiUlid01KDP3JTB7DDH46Y6CWBKHBFMR

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

P.F.C. Σ10603295240167
P.F.C. Σ10603295240389
P.F.C. Σ10603295240488
P.F.C. Σ10603295240310
P.F.C. Σ10603295240471
P.F.C. Σ10603295240235
P.F.C. Σ10603295240327
P.F.C. Σ10603295240204
P.F.C. Σ10603295240181
P.F.C. Σ10603295240365
P.F.C. Σ10603295240242
P.F.C. Σ10603295240433
P.F.C. Σ10603295240259
P.F.C. Σ10603295240297
P.F.C. Σ10603295240198
P.F.C. Σ10603295240426
P.F.C. Σ10603295240266
P.F.C. Σ10603295240440
P.F.C. Σ10603295240372
P.F.C. Σ10603295240150
P.F.C. Σ10603295240358
P.F.C. Σ10603295240419
P.F.C. Σ10603295240303