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SampLok® Sampling Kit 20mL

EUDAMEDFDA UDI

Class A (EU MDR)

Ref A100754

by ITL Asia Pacific Sdn. Bhd.

Identity

Trade Name
SampLok® Sampling Kit 20mL EUDAMED
SampLok® Sampling Kit 20mL FDA UDI
Generic Name
Blood/blood culture specimen transfer spike IVD, manual FDA UDI
Device Name
SampLok Sampling Kit EUDAMED
SampLok® Sampling Kit (SSK) - 20mL is used to transfers samples from blood bags or other containers with sterile docking compatible tubing to vacuum containers for laboratory tests. FDA UDI
Model / Reference
A100754 EUDAMEDFDA UDI
Description
SampLok® Sampling Kit (SSK) - 20mL is used to transfers samples from blood bags or other containers with sterile docking compatible tubing to vacuum containers for laboratory tests. FDA UDI

Identifiers

Catalog Number
A100754 FDA UDI
Primary DI / UDI-DI
09555240404084 EUDAMEDFDA UDI
Basic UDI-DI
955524040SSKSLJ EUDAMED
FDA Product Code
KSS FDA UDI
EMDN Code
W05019099 SAMPLES COLLECTION DEVICES - OTHER EUDAMED
GMDN Term
Blood/blood culture specimen transfer spike IVD, manual FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.9050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

SampLok® Sampling Kit 20mL by Itl Asia Pacific Sdn. Bhd. — 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

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Manufacturer

EUDAMED SRN
MY-MF-000001570
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED deb8d0d5-f3ce-4b88-8bb2-4b3ed66ba668 61 fields · synced Jul 9, 2026
  • FDA UDI 6fb64f6d-dfae-4395-9015-1da3348f5fa4 36 fields · synced May 30, 2026