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SMARTeZ Fluid Transfer Set

FDA UDI

Class I (US FDA UDI)

by Epic International(thailand) Company Limited

Identity

Trade Name
SMARTeZ Fluid Transfer Set FDA UDI
Generic Name
Fluid transfer set, general-purpose FDA UDI
Device Name
SMARTeZ Fluid Transfer Set (Tube Length 30cm) FDA UDI
Model / Reference
470020 FDA UDI
Description
SMARTeZ Fluid Transfer Set (Tube Length 30cm) FDA UDI

Identifiers

Primary DI / UDI-DI
18859299180028 FDA UDI
FDA Product Code
KYX FDA UDI
GMDN Term
Fluid transfer set, general-purpose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

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

Category: Fluid transfer set, general-purpose

SMARTeZ Fluid Transfer Set by Epic International(thailand) Company Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluid transfer set, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 679a4572-0a57-4280-af3d-f162eafa64da 33 fields · synced Jun 8, 2026