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Belgium· BE-AMP-SAM348311-00

GE Healthcare Chromium (51Cr) EDTA 3.7 MBq/ml

A 51cr-chromedetat product containing chrome (cr-51) edetate, registered in Belgium by GE Healthcare. The same ATC class is registered in 2 of our 19 countries.

ATC V09CX04

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedGE Healthcare Chromium (51Cr) EDTA 3.…ATCV09CX04REGISTER NO.BE-AMP-SAM348311-00PACKS LISTED1CHECKEDSeptember 26, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about chrome (cr-51) edetateAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

51cr-chromedetat is registered in 2 of 19 countries.

Countries holding a registration under ATC V09CX04 (51cr-chromedetat), each read from that country’s own register.

  • This record: Belgium, from FAMHP / AFMPS (Belgium)
  • 2 of them publish a price we can compare per daily dose
Search 51cr-chromedetat products by name

51cr-chromedetat · ATC V09CX04

2 / 19 countries

  • Belgiumprice
  • Finlandprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

FAMHP / AFMPS (Belgium)
Active substance
Chrome (Cr-51) Edetate
Manufacturer
GE Healthcare
Country
Belgium (BE)
ATC code
V09CX04
ATC class
51Cr-Chromedetat
Reimbursed
Not published by this register
Source register
FAMHP / AFMPS (Belgium)
Last checked
September 26, 2026

Packs & prices · 1

  • be_apb
    3335585

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same class

Other records under V09CX04

51cr-chromedetat, as other registers publish it.

All 51cr-chromedetat products

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FAMHP / AFMPS (Belgium). 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/6f128247-9001-46b7-acef-6d4864401984
GET /v1/drugs/6f128247-9001-46b7-acef-6d4864401984?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 injection",
  "source": "afmps",
  "status": "REVOKED",
  "name_en": "GE Healthcare Chromium (51Cr) EDTA 3.7 MBq/ml",
  "name_fr": "GE Healthcare Chromium (51Cr) EDTA 3.7 MBq/ml",
  "name_nl": "GE Healthcare Chromium (51Cr) EDTA 3.7 MBq/ml",
  "amp_code": "SAM348311-00",
  "strengths": [
    "3.7000",
    "3.7000"
  ],
  "pack_count": 1,
  "substances": [
    "Chrome (Cr-51) Edetate"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": "Chromium (51cr) Edetate",
  "authorisation_numbers": [
    "BE348311"
  ]
}
API referenceMCP serverPlans

See everything about 51cr-chromedetat.

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.

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