PGDx elio™ plasma focus Dx

Primary DI
00192721001494
Brand
PGDx elio™ plasma focus Dx
Company
PERSONAL GENOME DIAGNOSTICS INC.
Model
B01103102
Catalog number
B01103102
Device description
PGDx elio™ plasma focus Dx software
Published
2026-05-07
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
SBYHigh Throughput Sequencing Based Tumor Profiling Test Of Circulating Cell-Free Nucleic Acids

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
SBYHigh Throughput Sequencing Based Tumor Profiling Test Of Circulating Cell-Free Nucleic AcidsPathology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
DEN230046000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
DEN230046000PGDx elio plasma focus DxPersonal Genome Diagnostics, Inc.2024-08-01SBY

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00192721001494PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00192721001494001927210014941927210014940192721001494

GMDN Terms#

Term, Definition table
TermDefinition
Cancer-related multiple gene mutation/mRNA expression IVD, kit, nucleic acid technique (NAT)A collection of reagents and other associated materials intended for the qualitative and/or quantitative detection of mRNA expression and/or determination of the gene mutation status of multiple genes associated with cancer in a clinical specimen, using a nucleic acid technique (NAT). It is intended to be used in one or more of the following: select treatment options; predict or monitor the response to cancer therapy; risk assessment of cancer development, recurrence or metastasis; and/or for tumour profiling (e.g., cell-free DNA or circulating tumour DNA screening).

Regulatory Flags#

DUNS number
963427120
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
true
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00192721001463PGDx elio™ plasma focus DxA0310602A03106022026-05-07
00192721001449PGDx elio™ serverB-01-30800B-01-308002020-11-17
00192721001456PGDx elio™ serverB-01-40800B-01-408002020-11-17
00192721001432PGDx elio™ serverB-01-20800B-01-208002020-07-08
00192721000756PGDx elio™ serverB-01-10800B-01-108002020-05-11
00192721000763PGDx elio™ platformB0110900B01109002020-05-11
00192721000770PGDx elio™ tissue completeB01103200B011032002020-05-11
00192721001418PGDx elio™ tissue completeA0320100A03201002020-05-11
00192721001241PGDx elio™ diversiPhiA0840101A08401012020-05-11

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00192721001463PGDx elio™ plasma focus DxPERSONAL GENOME DIAGNOSTICS INC.SBY2026-05-07