← Back to catalogue

DOCTOR´S KIT DKS RhD-25

FDA UDI

Class II (US FDA UDI)

by Eldon Biologicals A/S

Identity

Trade Name
DOCTOR´S KIT DKS RhD-25 FDA UDI
Generic Name
Anti-Rh(D) red blood cell grouping IVD, antibody FDA UDI
Device Name
For 75 RhD blood group determinations. 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
660-01v05 FDA UDI
Description
For 75 RhD blood group determinations. 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
660-01 FDA UDI
Primary DI / UDI-DI
05713494000085 FDA UDI
510(k) Number
K790282 FDA UDI
FDA Product Code
KSZ FDA UDI
GMDN Term
Anti-Rh(D) red blood cell grouping IVD, antibody FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9175 FDA UDI
Commercial Distribution
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

Category: Anti-Rh(D) red blood cell grouping IVD, antibody

DOCTOR´S KIT DKS RhD-25 by Eldon Biologicals A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anti-Rh(D) red blood cell grouping IVD, antibody.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 9bf073e0-94cf-4cd6-a38c-7c5a19240c40 37 fields · synced May 30, 2026