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IMMULITE 2000 rPru av 3 Specific Allergen

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 10471074Model IVDR_67_LLB_DUB-C_B_REAG_rPru av 3 Specific Allergen

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
IMMULITE 2000 rPru av 3 Specific Allergen EUDAMEDFDA UDI
Generic Name
Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent FDA UDI
Device Name
IVDR_67_LLB_DUB-C_B_REAG_rPru av 3 Specific Allergen EUDAMED
rPru av 3 Allergen FDA UDI
Model / Reference
10471074 EUDAMEDFDA UDI
IVDR_67_LLB_DUB-C_B_REAG_rPru av 3 Specific Allergen EUDAMED
Description
rPru av 3 Allergen FDA UDI

Identifiers

Catalog Number
A599L2 FDA UDI
Primary DI / UDI-DI
00630414006253 EUDAMEDFDA UDI
Basic UDI-DI
0405686900629VR EUDAMED
510(k) Number
K132801 FDA UDI
FDA Product Code
DHB FDA UDI
EMDN Code
W01020202 IMMUNOGLOBULIN E - SPECIFIC, MONOTEST/MONORESULT EUDAMED
GMDN Term
Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent FDA UDI

Classification

Device Class
Class B EUDAMED
Class II FDA UDI
Regulation Number
866.5750 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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: Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent

IMMULITE 2000 rPru av 3 Specific Allergen by Siemens Healthcare Diagnostics Products Ltd — Class II — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 79efce9b-ed81-4abe-91ae-2d89115784d3 37 fields · synced Jun 19, 2026
  • EUDAMED 8140ec2c-b731-4576-8adc-9ede597820a4 61 fields · synced Jun 14, 2026