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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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Posterior Femoral Augment Trial — 11 UDI-DI variants, MDR

MD Atlas
DePuy Ireland UC

Data from EUDAMED, last updated May 24, 2026

Posterior Femoral Augment Trial

0603295a001638K

11 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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0603295a001638K
Device name: Posterior Femoral Augment Trial
Device model: PFC SIGMA Posterior Femoral Augment 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

11 UDI-DI variants

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Applied filters

basicUdiUlid01KDP3K77VH7Q41TX8SV2NNN06

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. Σ10603295240228
P.F.C. Σ10603295240341
P.F.C. Σ10603295240402
P.F.C. Σ10603295240464
P.F.C. Σ10603295240334
P.F.C. Σ10603295240273
P.F.C. Σ10603295240174
P.F.C. Σ10603295240457
P.F.C. Σ10603295240396
P.F.C. Σ10603295240280
P.F.C. Σ10603295240211