← Back to catalogue

Polymer Pouch Caps, Dx

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 4462785

by Life Technologies Holdings Pte Ltd

Identity

Trade Name
Polymer Pouch Caps, Dx EUDAMED
3500Dx Series Polymer Pouch Caps FDA UDI
Generic Name
Test tube/reservoir cap IVD FDA UDI
Device Name
Polymer Pouch Cap, a part of Genetic Analyzer Reagents and Consumables EUDAMED
KIT,POUCH CAP IVD 3500 FDA UDI
Model / Reference
4462785 EUDAMEDFDA UDI
Description
KIT,POUCH CAP IVD 3500 FDA UDI

Identifiers

Primary DI / UDI-DI
10190302000680 EUDAMEDFDA UDI
Basic UDI-DI
01903024462785CK EUDAMED
FDA Product Code
PCA FDA UDI
EMDN Code
W02050185 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - CONSUMABLES EUDAMED
GMDN Term
Test tube/reservoir cap 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

Polymer Pouch Caps, 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 c4c079f4-f12b-4995-b5fb-85c7c05150ed 61 fields · synced Jul 26, 2026
  • FDA UDI 8b54889e-58e4-443b-b10a-de9768f6402b 33 fields · synced May 30, 2026