← Back to catalogue

Septa Cathode Buffer Container Dx

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 4410716

by Life Technologies Holdings Pte Ltd

Identity

Trade Name
Septa Cathode Buffer Container Dx EUDAMED
SEPTA, Cathode Buffer CNTR 3500 FDA UDI
Generic Name
Buffered sample diluent IVD FDA UDI
Device Name
Septa Cathode Buffer Container, a part of Genetic Analyzer Reagents and Consumables EUDAMED
SEPTA CATHODE BUFFER CNTR 3500 FDA UDI
Model / Reference
4410716 EUDAMEDFDA UDI
Description
SEPTA CATHODE BUFFER CNTR 3500 FDA UDI

Identifiers

Primary DI / UDI-DI
10190302000277 EUDAMEDFDA UDI
Basic UDI-DI
019030244107169T EUDAMED
FDA Product Code
PCA FDA UDI
EMDN Code
W02050185 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - CONSUMABLES EUDAMED
GMDN Term
Buffered sample diluent IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class II FDA UDI
Regulation Number
862.2570 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Septa Cathode Buffer Container Dx by Life Technologies Holdings Pte Ltd. — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
SG-MF-000023931
Authorised Representative
Life Technologies Europe B.V. NL-AR-000021890

Sources (2)

  • EUDAMED b9e961e9-193e-44ef-948a-4d7aec591c49 61 fields · synced Jul 24, 2026
  • FDA UDI 1830a522-517a-4a39-b743-51eaade3e399 33 fields · synced May 30, 2026