← Back to catalogue

Astoflo® Plus Eco

FDA UDI

Class II (US FDA UDI)

by Stihler Electronic GmbH

Identity

Trade Name
ASTOFLO® PLUS ECO FDA UDI
Generic Name
Conduction blood/fluid warmer FDA UDI
Device Name
Heating profile FDA UDI
Model / Reference
WP31 FDA UDI
Description
Heating profile FDA UDI

Identifiers

Catalog Number
WP31 FDA UDI
Primary DI / UDI-DI
04260114140672 FDA UDI
510(k) Number
K082765 FDA UDI
FDA Product Code
LGZ FDA UDI
GMDN Term
Conduction blood/fluid warmer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 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

Astoflo® Plus Eco 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c2bd4a1f-ffc0-4451-8b02-762cf0bd8cbc 35 fields · synced May 30, 2026