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Astotube®

FDA UDI

Class II (US FDA UDI)

by Stihler Electronic GmbH

Identity

Trade Name
ASTOTUBE® FDA UDI
Generic Name
Intravenous administration tubing extension set FDA UDI
Device Name
PVC infusion extension FDA UDI
Model / Reference
IFT30410 FDA UDI
Description
PVC infusion extension FDA UDI

Identifiers

Catalog Number
IFT30410 FDA UDI
Primary DI / UDI-DI
04260114140641 FDA UDI
510(k) Number
K991160 FDA UDI
FDA Product Code
BSB FDA UDI
GMDN Term
Intravenous administration tubing extension set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9205 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intravenous administration tubing extension set

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

Similar devices

Also classified as Intravenous administration tubing extension set.

Cleared under the same submission

K991160 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stihler Electronic GmbH

Sources (1)

  • FDA UDI a280f91c-c3dc-4e9b-b92b-37ac683e262e 36 fields · synced May 30, 2026