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Human CH50 Reagent pack for use on the SPAPLUS

FDA UDI

Class II (US FDA UDI)

by The Binding Site Group

Identity

Trade Name
Human CH50 Reagent pack for use on the SPAPLUS FDA UDI
Generic Name
Total complement activity (CH50) IVD, reagent FDA UDI
Model / Reference
NK095.S FDA UDI

Identifiers

Primary DI / UDI-DI
05051700015592 FDA UDI
FDA Product Code
DAE FDA UDI
GMDN Term
Total complement activity (CH50) IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5240 FDA UDI
Commercial Distribution
Not 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

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

Human CH50 Reagent pack for use on the SPAPLUS by The Binding Site Group — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 73bc95a2-57ec-48e3-8f8a-05e43e2a114a 35 fields · synced Jun 8, 2026