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C3 Control Cells

FDA UDI

Class II (US FDA UDI)

by Hemo Bioscience

Identity

Trade Name
C3 Control Cells FDA UDI
Generic Name
Complement coated reagent red blood cell IVD, control FDA UDI
Device Name
C3 Control Cells are used to confirm the reactivity of anti-C3 in Anti-human globulin. FDA UDI
Model / Reference
H9000 FDA UDI
Description
C3 Control Cells are used to confirm the reactivity of anti-C3 in Anti-human globulin. FDA UDI

Identifiers

Catalog Number
H9000 FDA UDI
Primary DI / UDI-DI
00858352006016 FDA UDI
FDA Product Code
KSF FDA UDI
GMDN Term
Complement coated reagent red blood cell IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9650 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

Yes

FDA UDI

Prescription Use

Yes

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

Category: Complement coated reagent red blood cell IVD, control

C3 Control Cells by Hemo Bioscience — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Complement coated reagent red blood cell IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hemo Bioscience

Sources (1)

  • FDA UDI 839b8381-86d1-4fba-ae2d-ee0f62f3c649 36 fields · synced Jun 8, 2026