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iLet Connect Adapter

FDA UDI

Class II (US FDA UDI)

by Beta Bionics, Inc.

Identity

Trade Name
iLet Connect Adapter FDA UDI
Generic Name
Luer/Luer linear connector, single-use FDA UDI
Device Name
For use with the iLet Bionic Pancreas FDA UDI
Model / Reference
Insulin Only FDA UDI
Description
For use with the iLet Bionic Pancreas FDA UDI

Identifiers

Catalog Number
BB3010 FDA UDI
Primary DI / UDI-DI
00850050080091 FDA UDI
FDA Product Code
QFG FDA UDI
GMDN Term
Luer/Luer linear connector, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

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: Luer/Luer linear connector, single-use

iLet Connect Adapter by Beta Bionics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer/Luer linear connector, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Beta Bionics, Inc.

Sources (1)

  • FDA UDI b6d9a677-1c4b-45ac-b360-a3763d50ef54 35 fields · synced Jun 8, 2026