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YSI Incorporated

FDA UDI

Class II (US FDA UDI)

by Ysi Incorporated

Identity

Trade Name
YSI Incorporated FDA UDI
Generic Name
Glucose IVD, calibrator FDA UDI
Device Name
2747 DUAL STANDARD (CALIBRATOR) FDA UDI
Model / Reference
2747 FDA UDI
Description
2747 DUAL STANDARD (CALIBRATOR) FDA UDI

Identifiers

Catalog Number
061827 FDA UDI
Primary DI / UDI-DI
00851683007004 FDA UDI
FDA Product Code
CGA FDA UDI
GMDN Term
Glucose IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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: Glucose IVD, calibrator

YSI Incorporated by Ysi Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ysi Incorporated

Sources (1)

  • FDA UDI fc56f844-994f-405a-9fc9-0bd31d357fa9 34 fields · synced Jun 8, 2026