Ireland· IE-PA-EU/1/17/1239/003-004
VeraSeal 80 mg/ml/500 IU/ml Solutions for sealant
A local hemostatics product containing human fibrinogen, registered in Ireland by Instituto Grifols S.A.. The same ATC class is registered in 7 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
Human fibrinogen is registered in 7 of 19 countries.
Countries holding a registration under ATC B02BC (local hemostatics), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 6 of them publish a price we can compare per daily dose
Human fibrinogen · ATC B02BC
7 / 19 countries
- Belgiumprice
- Finlandprice
- Icelandprice
- Ireland
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
HPRA (Ireland)- Active substance
- Human fibrinogen
- Manufacturer
- Instituto Grifols S.A.
- Country
- Ireland (IE)
- ATC code
- B02BC
- ATC class
- Local hemostatics
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberEU/1/17/1239/003-004
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Human fibrinogen in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomARTISS solution for sealant 10ml pre-filled syringesBaxter Healthcare Ltd
- BelgiumArtissBaxter
- SpainFIBCLOT 1,5 G POLVO Y DISOLVENTE PARA SOLUCION INYECTABLE Y PARA PERFUSIONLaboratoire Francais Du Fractionnement Et Des Biotechnologies
- GermanyFibclotLaboratoire Francais Du Fractionnement Et Des Biotechnologies
- FinlandFibclotLaboratoire Francais du Fractionnement et des Biotechnologies
- NetherlandsFibclot 1,5 g, poeder en oplosmiddel voor oplossing voor injectie/infusieLaboratoire Francais Du Fractionnement Et Des Biotechnologies
- SwedenFibclot 1,5 g Pulver och vätska till injektions-/infusionsvätska, lösningLaboratoire français du Fractionnement et des Biotechnologies
- CzechiaFIBRYGAOctapharma (IP) SPRL, Anderlecht
Authorised across Europe · EMA
The same active substance is authorised in 29 EEA countries. Names it is sold under:
- Austria · Fibclot, Fibryga
- Belgium · Fibclot, Fibryga
- Bulgaria · Fibryga, Хемокомплетан P
- Cyprus · Fibryga, Riastap
- Czechia · Fibryga, Haemocomplettan P
- Germany · Fibclot, Fibryga
- Denmark · Fibclot, Fibryga
- Estonia · Fibryga
- Spain · Fibclot, Fibryga
- Finland · Fibclot, Fibryga
- France · Clottafact, Fibryga
- United Kingdom (Northern Ireland) · Fibclot, Fibryga
- Greece · Fibclot, Riastap
- Croatia · Fibryga
- Hungary · Fibclot, Fibryga
- Iceland · Fibryga, Riastap
- Italy · Fibriclotte, Fibryga
- Lithuania · Fibryga
- Luxembourg · Fibclot, Fibryga
- Latvia · Fibryga
- Malta · Fibryga, Riastap
- Netherlands · Fibclot, Fibryga
- Norway · Fibclot, Fibryga
- Poland · Fibryga, Riastap
- Portugal · Fibryga, Haemocomplettan
- Romania · Fibryga, Haemocomplettan P
- Sweden · Fibclot, Fibryga
- Slovenia · Fibrema, Prufibry
- Slovakia · Fibryga, Riastap
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of HPRA (Ireland). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/ad5a95bd-8219-40ad-a4d8-a50d5d6024ea GET /v1/drugs/ad5a95bd-8219-40ad-a4d8-a50d5d6024ea?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"form": "Solution for sealant",
"routes": [
"Epilesional use"
],
"source": "hpra",
"atc_all": [
"B02BC"
],
"strength": null,
"pa_number": "EU/1/17/1239/003-004",
"substances": [
"Human fibrinogen"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Unknown",
"authorised_at": "10/11/2017",
"dispensing_status": "Product subject to prescription which may not be renewed (A)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}See everything about human fibrinogen.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.