Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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.

Organization name
UDI-DI code
Reference / catalog number

HAMD6 — Class III MDD by Instituto de…

MD Atlas
Instituto de Investigación Biotecnológica, Farmacéutica y Medicamentos Huérfanos, S.L.

EUDAMED last updated this device on Feb 18, 2026

HAMD6

B-843655523221G3WM

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Instituto de Investigación Biotecnológica, Farmacéutica y Medicamentos Huérfanos, S.L.
UDI-DI code: D-843655523221G3WM
Reference / catalog number: HAMD6

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?

Manufacturer information

Organization name: Instituto de Investigación Biotecnológica, Farmacéutica y Medicamentos Huérfanos, S.L.
SRN: ES-MF-000001065
Manufacturer status: Active

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW011
Professional use
CW010
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	May 18, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: D-843655523221G3WM
Basic UDI-DI: B-843655523221G3WM
Reference / catalog number: HAMD6
Issuing entity: EUDAMED

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

T21475B-843655523214G6X3On the market HAMD1B-843655523217GCYAOn the market HAMD2B-843655523215G8XCOn the market HAMD4B-843655523219GGYUOn the market HAMD5B-843655523220FZYROn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.