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Xpression Box

FDA UDI

Class I (US FDA UDI)

by Intra-Lock International

Identity

Trade Name
Xpression Box FDA UDI
Generic Name
Haematological concentrate system FDA UDI
Device Name
Xpression Box FDA UDI
Model / Reference
CTR FDA UDI
Description
Xpression Box FDA UDI

Identifiers

Catalog Number
CTR FDA UDI
Primary DI / UDI-DI
D742CTR0 FDA UDI
FDA Product Code
EKF FDA UDI
GMDN Term
Haematological concentrate system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Haematological concentrate system

Xpression Box by Intra-Lock International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haematological concentrate system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Intra-Lock International

Sources (1)

  • FDA UDI 017ce77c-92e8-4018-a63f-1df10f1c8296 35 fields · synced May 30, 2026