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Prismaflo® Ii S

FDA UDI

Class II (US FDA UDI)

by Stihler Electronic GmbH

Identity

Trade Name
PRISMAFLO® II S FDA UDI
Generic Name
Conduction blood/fluid warmer FDA UDI
Device Name
Blood warmer FDA UDI
Model / Reference
PF2300NA FDA UDI
Description
Blood warmer FDA UDI

Identifiers

Catalog Number
PF2300NA FDA UDI
Primary DI / UDI-DI
04260114149897 FDA UDI
510(k) Number
K082758 FDA UDI
FDA Product Code
KOC FDA UDI
GMDN Term
Conduction blood/fluid warmer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Conduction blood/fluid warmer

Prismaflo® Ii S by Stihler Electronic GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Conduction blood/fluid warmer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9b0f8ab2-71b6-46af-9ebd-ce5f150a1a15 35 fields · synced May 31, 2026