Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002807751

FEI Number

3002807751

Entity Name

NOVO NORDISK A/S

City/State/Country

Kalundborg Sjalland, DK

Establishment Address

Hallas Alle 1, Kalundborg Sjalland 4400, DK

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

NOVO NORDISK INC. (Owner Number: 9027307)

Owner / Operator Contact Address

800 Scudders Mill Road, Plainsboro, NJ 08536, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Administration Set

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRS	I.V. Start Kit	General Hospital	Class 2	880.5200	2007-11-29

Official Correspondent

Rinku Sur

US Agent Details

Prabhdeep Singh Business: NOVO NORDISK INC. Email: prsi@novonordisk.com Phone: (609) 9875439

Related Public Records

Same Entity

NOVO NORDISK INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3005186124	Novo Nordisk (China) Pharmaceuticals, Co. Ltd.	Tianjin, CN
2244771	NOVO NORDISK INC.	Plainsboro, NJ, US
9681821	NOVO NORDISK A/S	HILLEROED Hovedstaden, DK
9681822	NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI	HJOERRING Nordjylland, DK

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1423395	MEDLINE INDUSTRIES, LP - SPT	Waukegan, IL, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002807751. Last updated year: 2026. Please use registration number 3002807751 when referencing this establishment in official correspondence.