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Para 4

FDA UDI

Class II (US FDA UDI)

by Streck

Identity

Trade Name
Para 4 FDA UDI
Generic Name
Full blood count IVD, control FDA UDI
Device Name
A multi-parameter hematology control for small laboratories and point-of-care applications that perform a limited number of hematology tests. Contains 2 vials each of low & normal levels. FDA UDI
Model / Reference
215110 FDA UDI
Description
A multi-parameter hematology control for small laboratories and point-of-care applications that perform a limited number of hematology tests. Contains 2 vials each of low & normal levels. FDA UDI

Identifiers

Catalog Number
215110 FDA UDI
Primary DI / UDI-DI
00844509000723 FDA UDI
510(k) Number
K842017 FDA UDI
FDA Product Code
JPK FDA UDI
GMDN Term
Full blood count IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.8625 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 1.5 Milliliter FDA UDI

Category: Full blood count IVD, control

Para 4 by Streck — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Full blood count IVD, control.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Streck

Sources (1)

  • FDA UDI b6489dbb-c62f-4599-8c54-12a9025366a0 38 fields · synced Jun 6, 2026