Diana Peristaltic Pump Module, Refurbished

FDA UDI

Class II (US FDA UDI)

by Icu Medical, Inc.

Identity

Trade Name: Diana Peristaltic Pump Module, Refurbished FDA UDI
Generic Name: Pharmaceutical fluid-dispensing system FDA UDI
Device Name: Diana Peristaltic Pump Module, Refurbished FDA UDI
Model / Reference: DS1000R FDA UDI
Description: Diana Peristaltic Pump Module, Refurbished FDA UDI

Identifiers

Catalog Number: DS1000R FDA UDI
Primary DI / UDI-DI: 00887709122697 FDA UDI
FDA Product Code: NEP FDA UDI
GMDN Term: Pharmaceutical fluid-dispensing system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5440 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pharmaceutical fluid-dispensing system

Diana Peristaltic Pump Module, Refurbished by Icu Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Icu Medical, Inc.

Sources (1)

FDA UDI bfa332f3-8600-4297-8c3e-e108f670e873 36 fields · synced May 29, 2026