Eu Ivdr Eu Ivd Class B On The Market ๐Ÿ‡จ๐Ÿ‡ฟ Czechia

Ultra-Sensitive Estradiol RIA

IMMUNOTECH s.r.o. ยท ๐Ÿ‡จ๐Ÿ‡ฟ Czechia
Devices (same UDI-DI)
1
Certificates
0
Countries
12
Notified Bodies
0

Basic Information

Primary DI
15099590211523
Basic UDI-DI Code
150995905DSL4800FP
Reference
DSL4800
Device Types
None provided
Regulation
Eu Ivdr
Classification
Eu Ivd Class B
Status
On The Market
Manufacturer
IMMUNOTECH s.r.o.

Additional Description

Ultra-Sensitive Estradiol RIA is an in vitro diagnostic manual medical device intended to be used by healthcare professionals for the quantitative measurement of estradiol in human serum and plasma. Measurement of estradiol is intended to be used for the assessment of fertility status and sexual development. In females, it is used in differential diagnosis of amenorrhea and other causes of female infertility and in monitoring of ovulation status. It is also used as an aid in diagnosis of precocious and delayed puberty in children. In males, it is used as an aid in diagnosis of feminizing syndromes, including gynecomastia. It is also used in monitoring patients on hormone replacement and antiestrogen therapy.

CND Nomenclature Codes

Code Description
W0102050103 ESTRADIOL

Available In Countries

๐Ÿ‡ฆ๐Ÿ‡น Austria ๐Ÿ‡ง๐Ÿ‡ช Belgium ๐Ÿ‡จ๐Ÿ‡ฟ Czechia ๐Ÿ‡ฉ๐Ÿ‡ช Germany ๐Ÿ‡ช๐Ÿ‡ธ Spain ๐Ÿ‡ซ๐Ÿ‡ท France ๐Ÿ‡ญ๐Ÿ‡บ Hungary ๐Ÿ‡ฎ๐Ÿ‡ช Ireland ๐Ÿ‡ฎ๐Ÿ‡น Italy ๐Ÿ‡ฒ๐Ÿ‡น Malta ๐Ÿ‡ต๐Ÿ‡ฑ Poland ๐Ÿ‡ธ๐Ÿ‡ฐ Slovakia

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