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Tandem t:slim Autosoft 30 kit

FDA UDI

Class II (US FDA UDI)

by Tandem Diabetes Care, Inc.

Identity

Trade Name
Tandem t:slim Autosoft 30 kit FDA UDI
Generic Name
Ambulatory insulin infusion pump reservoir FDA UDI
Device Name
Tandem t:slim ASFT30 PK14 23" FDA UDI
Model / Reference
1017076 FDA UDI
Description
Tandem t:slim ASFT30 PK14 23" FDA UDI

Identifiers

Primary DI / UDI-DI
00389152707679 FDA UDI
510(k) Number
K232380 FDA UDI
K232382 FDA UDI
FDA Product Code
QJI FDA UDI
QFG FDA UDI
GMDN Term
Ambulatory insulin infusion pump reservoir FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1356 FDA UDI
880.5730 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

Yes

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: Electric infusion pump administration set, single-useAmbulatory insulin infusion pump, electronic, software-dosing, scalar algorithmAmbulatory insulin infusion pump reservoir

Tandem t:slim Autosoft 30 kit by Tandem Diabetes Care, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulatory insulin infusion pump reservoir.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b238982a-cd96-4a73-bf63-1797d04437ee 34 fields · synced Jun 8, 2026