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Intra-Lock

FDA UDI

Class I (US FDA UDI)

by Intra-Lock International

Identity

Trade Name
Intra-Lock FDA UDI
Generic Name
Haematological concentrate system FDA UDI
Device Name
Piston for Xpression Box FDA UDI
Model / Reference
PXB FDA UDI
Description
Piston for Xpression Box FDA UDI

Identifiers

Catalog Number
PXB FDA UDI
Primary DI / UDI-DI
D742PXB0 FDA UDI
FDA Product Code
NVG FDA UDI
GMDN Term
Haematological concentrate system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.2240 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

Intra-Lock 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

Sources (1)

  • FDA UDI dd850c5d-43c0-4094-a823-51e8cbdffc11 34 fields · synced May 31, 2026