← Back to catalogue

Medtronic MiniMed Pro-Set Infusion Set, PCAP Connection 42in

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
Medtronic MiniMed Pro-Set Infusion Set, PCAP Connection 42in FDA UDI
Generic Name
Electric infusion pump administration set, single-use FDA UDI
Device Name
MINIMED 42IN PCAP MMT-281600 FDA UDI
Model / Reference
328617 FDA UDI
Description
MINIMED 42IN PCAP MMT-281600 FDA UDI

Identifiers

Catalog Number
328617 FDA UDI
Primary DI / UDI-DI
00382903286171 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Electric infusion pump administration set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
Not 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 42 Inch FDA UDI

Medtronic MiniMed Pro-Set Infusion Set, PCAP Connection 42in by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID

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 e4ba588f-4ada-4d64-9969-3a41d54a39df 36 fields · synced Jun 8, 2026