Ireland· IE-PA-PA0690/010/001
Technescan PYP 20 mg kit for radiopharmaceutical preparation
A 99mtc-technetium-zinn markierte zellen product containing sodium pyrophosphate decahydrate + stannous chloride dihydrate, registered in Ireland by Curium Netherlands B.V.. The same ATC class is registered in 8 of our 19 countries.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
Where it is registered
99mtc-technetium-zinn markierte zellen is registered in 8 of 19 countries.
Countries holding a registration under ATC V09GA06 (99mtc-technetium-zinn markierte zellen), each read from that country’s own register.
- This record: Ireland, from HPRA (Ireland)
- 4 of them publish a price we can compare per daily dose
99mtc-technetium-zinn markierte zellen · ATC V09GA06
8 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Ireland
- Netherlands
- Polandprice
The record
At a glance
HPRA (Ireland)- Active substance
- Sodium pyrophosphate decahydrate + Stannous chloride dihydrate
- Manufacturer
- Curium Netherlands B.V.
- Country
- Ireland (IE)
- ATC code
- V09GA06
- ATC class
- 99mTc-Technetium-Zinn markierte Zellen
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberPA0690/010/001
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
99mtc-technetium-zinn markierte zellen in 1 other country
What each register calls a product with the same active substance — salts and hydrates count as the same.
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Belgium · Technescan Pyp
- Norway · Technescan Pyp
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/c5454dcb-f150-4eb8-ad46-afe33041ed21 GET /v1/drugs/c5454dcb-f150-4eb8-ad46-afe33041ed21?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": "Kit for radiopharmaceutical preparation",
"routes": [
"Intravenous use"
],
"source": "hpra",
"atc_all": [
"V09GA",
"V09GA06"
],
"strength": null,
"pa_number": "PA0690/010/001",
"substances": [
"Sodium pyrophosphate decahydrate",
"Stannous chloride dihydrate"
],
"legal_basis": "Well-established use application (Article 10a of Directive No 2001/83/EC)",
"market_info": "Marketed",
"authorised_at": "29/06/2001",
"dispensing_status": "Product subject to Restricted Prescription (C)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}See everything about 99mtc-technetium-zinn markierte zellen.
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.