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.

HYALOTEND — 1 UDI-DI variant, MDD (Fidia Farmaceutici S.p.A.)

MD Atlas
Fidia Farmaceutici S.p.A.

Data from EUDAMED, last updated May 30, 2026

HYALOTEND

B-100001222G

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class III

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Manufacturer: Fidia Farmaceutici S.p.A.

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

Implantable

Clinical investigations

Registered: No

Legacy certificates

Certificate number: 8825
Type: refdata.legacy.mdd-certificate-type.v
Notified body: GMED SAS (0459)
Validity: Dec 31, 2027

Certificate number: 36522
Type: refdata.legacy.mdd-certificate-type.iii
Notified body: GMED SAS (0459)
Validity: Dec 31, 2027

Identity & classification

Basic UDI-DI: B-100001222G
Device name: HYALOTEND
Device model: EQP201_1A
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: Fidia Farmaceutici S.p.A.
SRN: IT-MF-000026988
Country: Italy
Email: agastaIdi@fidiapharma.it

Variants by status

UDI-DI variants

1 UDI-DI variant

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

basicUdiUlid01KQS12Y57P613Y5TCWBSZWXTC

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

10000122D-100001222G