United Kingdom MHRA device registration 207637
Evacuated blood collection tube IVD, anticoagulant/cell preservative
United Kingdom·In Vitro Diagnostic Device·Natera, Inc·Registered Dec 21, 2024DREGIYRegistration details
- Device ID
- 207637
- Status
- DREGIY
- Date Registered
- Dec 21, 2024
Device classification
- Device Type
- In Vitro Diagnostic Device
- Type
- IVD General
Manufacturer
- Name
- Natera, Inc
- Address
- 201 Industrial Road, Suite 410San Carlos, California, United States
Similar products
Devices with a matching generic name or device type registered with MHRA
Alpha-fetoprotein (AFP) IVD, kit, fluorescent immunoassayN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176179
Cyclic citrullinated peptide antibody (anti-CCP) IVD, kit, fluorescent immunoassayN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176185
Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinicalN/A
Type: In Vitro Diagnostic Device
Manufacturer: Primer Design Ltd
Device ID: 175386
Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, fluorescent immunoassayN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176184
C-reactive protein (CRP) IVD, kit, fluorescent immunoassayN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176164
Cryptosporidium species antigen IVD, kit, rapid ICT, clinicalN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176139
Respiratory syncytial virus (RSV) antigen IVD, kit, rapid ICT, clinicalN/A
Type: In Vitro Diagnostic Device
Manufacturer: Primer Design Ltd
Device ID: 175389
SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testingN/A
Type: In Vitro Diagnostic Device
Manufacturer: Primer Design Ltd
Device ID: 175394
Trichomonas vaginalis antigen IVD, kit, rapid ICT, clinicalN/A
Type: In Vitro Diagnostic Device
Manufacturer: Primer Design Ltd
Device ID: 175395
D-dimer IVD, kit, fluorescent immunoassayN/A
Type: In Vitro Diagnostic Device
Manufacturer: Vitrosens Biyoteknoloji A.S.
Device ID: 176162
Other products from Natera, Inc
Additional devices registered by the same manufacturer
Evacuated blood collection tube IVD, anticoagulantDec 21, 2024
Type: In Vitro Diagnostic Device
Device ID: 207636
Circulating tumour DNA/RNA IVD, kit, nucleic acid technique (NAT)Nov 26, 2024
Type: In Vitro Diagnostic Device
Device ID: 126005
Evacuated blood collection tube IVD, anticoagulantNov 26, 2024
Type: In Vitro Diagnostic Device
Device ID: 126002
Human genomic analysis interpretive softwareNov 26, 2024
Type: In Vitro Diagnostic Device
Device ID: 100008
Multiple congenital aneuploidy screening IVD, kit, nucleic acid technique (NAT)Nov 26, 2024
Type: In Vitro Diagnostic Device
Device ID: 100009
Nucleic acid amplification mastermix kit IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Device ID: 100010
Evacuated blood collection tube IVD, anticoagulant/cell preservativeNov 26, 2024
Type: In Vitro Diagnostic Device
Device ID: 126004
General specimen container IVD, no additive/mediumNov 26, 2024
Type: In Vitro Diagnostic Device
Device ID: 153862
Human genomic analysis interpretive software IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Device ID: 126006
Nucleic acid amplification primer IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Device ID: 100011
About this record
Evacuated blood collection tube IVD, anticoagulant/cell preservative is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207637. The device is manufactured by Natera, Inc from United States, classified as In Vitro Diagnostic Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Free DatabasePowered by Pure Global AIMHRA RegisteredIn Vitro Diagnostic Device