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Intra-Lock

FDA UDI

Class II (US FDA UDI)

by Intra-Lock International

Identity

Trade Name
Intra-Lock FDA UDI
Generic Name
Blood collection set, noninvasive FDA UDI
Device Name
L-PRF Red Cap Blood Collection CAT Tube (9 ml) FDA UDI
Model / Reference
BVBCTP2_50 FDA UDI
Description
L-PRF Red Cap Blood Collection CAT Tube (9 ml) FDA UDI

Identifiers

Catalog Number
BVBCTP2_50 FDA UDI
Primary DI / UDI-DI
D742BVBCTP250 FDA UDI
FDA Product Code
ORG FDA UDI
GMDN Term
Blood collection set, noninvasive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9245 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood collection set, noninvasive

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

Similar devices

Also classified as Blood collection set, noninvasive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 83c3bca7-7bd4-449b-a81c-f2b13f02cd7b 36 fields · synced May 31, 2026