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ADVIA® Autoslide Wright-Giemsa Stain

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
ADVIA® Autoslide Wright-Giemsa Stain FDA UDI
Generic Name
Phosphate buffer/Sorenson buffer solution IVD FDA UDI
Device Name
ADVIA® Autoslide Wright-Giema Stain FDA UDI
Model / Reference
10327572 FDA UDI
Description
ADVIA® Autoslide Wright-Giema Stain FDA UDI

Identifiers

Catalog Number
8097532 FDA UDI
Primary DI / UDI-DI
00630414503950 FDA UDI
FDA Product Code
HYF FDA UDI
GMDN Term
Phosphate buffer/Sorenson buffer solution IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1850 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: Phosphate buffer/Sorenson buffer solution IVD

ADVIA® Autoslide Wright-Giemsa Stain by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phosphate buffer/Sorenson buffer solution IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c581917f-2cef-439e-846b-6b4a82ad9025 36 fields · synced May 30, 2026