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IMMULITE® 2000 Systems INS Insulin Sample Diluent

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
IMMULITE® 2000 Systems INS Insulin Sample Diluent FDA UDI
Generic Name
Buffered sample diluent IVD FDA UDI
Device Name
Insulin Sample Diluent - IMMULITE - 1x25mL FDA UDI
Model / Reference
10387066 FDA UDI
Description
Insulin Sample Diluent - IMMULITE - 1x25mL FDA UDI

Identifiers

Catalog Number
L2INZ FDA UDI
Primary DI / UDI-DI
00630414954035 FDA UDI
510(k) Number
K022603 FDA UDI
FDA Product Code
CEW FDA UDI
GMDN Term
Buffered sample diluent IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1545 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® 2000 Systems INS Insulin 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 bdd48b3a-0fc5-41f6-904b-cc7b1d879948 37 fields · synced May 29, 2026