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IMMULITE®/IMMULITE® 1000 Systems BRM BR-MA Sample Diluent

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
IMMULITE®/IMMULITE® 1000 Systems BRM BR-MA Sample Diluent FDA UDI
Generic Name
Buffered sample diluent IVD FDA UDI
Device Name
CA 15-3 Sample Diluent - IMMULITE - 1x25mL FDA UDI
Model / Reference
10387018 FDA UDI
Description
CA 15-3 Sample Diluent - IMMULITE - 1x25mL FDA UDI

Identifiers

Catalog Number
LBRZ FDA UDI
Primary DI / UDI-DI
00630414953601 FDA UDI
510(k) Number
K013984 FDA UDI
FDA Product Code
MOI FDA UDI
GMDN Term
Buffered sample diluent IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.6010 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

No

FDA UDI

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: Buffered sample diluent IVD

IMMULITE®/IMMULITE® 1000 Systems BRM BR-MA Sample Diluent by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Buffered sample diluent IVD.

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 d7401763-4d02-436c-8191-eed7d9f94aeb 37 fields · synced May 31, 2026