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Administration Set

FDA UDI

Class II (US FDA UDI)

by Novo Nordisk Inc.

Identity

Trade Name
Administration Set FDA UDI
Generic Name
Percutaneous medicine administration kit, non-medicated, single-use FDA UDI
Device Name
Administration set for infusion containing 2 alcohol swabs, 1 infusion set, 2 gauze pads, and 2 bandages. FDA UDI
Model / Reference
720006 FDA UDI
Description
Administration set for infusion containing 2 alcohol swabs, 1 infusion set, 2 gauze pads, and 2 bandages. FDA UDI

Identifiers

Catalog Number
720006 FDA UDI
Primary DI / UDI-DI
00301697200064 FDA UDI
FDA Product Code
LRS FDA UDI
GMDN Term
Percutaneous medicine administration kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Percutaneous medicine administration kit, non-medicated, single-use

Administration Set by Novo Nordisk Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous medicine administration kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novo Nordisk Inc.

Sources (1)

  • FDA UDI 54bcba21-9d0c-4be2-b00a-44d828fd3e1c 36 fields · synced Jun 6, 2026