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Eldon School Kit Ska 2511-30

FDA UDI

Class II (US FDA UDI)

by Eldon Biologicals A/S

Identity

Trade Name
ELDON SCHOOL KIT SKA 2511-30 FDA UDI
Generic Name
ABO/Rh multiple blood grouping IVD, kit, agglutination FDA UDI
Device Name
For self-testing of ABO and RhD Blood groups. Not for use for screening purposes prior to transfusion. Dry format cards for ABO and/or RhD determination for the grouping of stabilized venous blood, capillary blood or washed red cells. FDA UDI
Model / Reference
504-32v03 FDA UDI
Description
For self-testing of ABO and RhD Blood groups. Not for use for screening purposes prior to transfusion. Dry format cards for ABO and/or RhD determination for the grouping of stabilized venous blood, capillary blood or washed red cells. FDA UDI

Identifiers

Catalog Number
504-32 FDA UDI
Primary DI / UDI-DI
05713494000382 FDA UDI
510(k) Number
K790282 FDA UDI
FDA Product Code
KSZ FDA UDI
GMDN Term
ABO/Rh multiple blood grouping IVD, kit, agglutination FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9175 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Eldon School Kit Ska 2511-30 by Eldon Biologicals A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 695c0654-073e-42ad-8f37-c824ebce87a2 38 fields · synced May 30, 2026