← Back to catalogue

Diana Peristaltic Pump Module

FDA UDI

Class II (US FDA UDI)

by Icu Medical, Inc.

Identity

Trade Name
Diana Peristaltic Pump Module FDA UDI
Generic Name
Pharmaceutical fluid-dispensing system FDA UDI
Device Name
Diana Peristaltic Pump FDA UDI
Model / Reference
DS1000 FDA UDI
Description
Diana Peristaltic Pump FDA UDI

Identifiers

Catalog Number
DS1000 FDA UDI
Primary DI / UDI-DI
00840619099046 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

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pharmaceutical fluid-dispensing system

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

Similar devices

Also classified as Pharmaceutical fluid-dispensing system.

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

Manufacturer
Icu Medical, Inc.

Sources (1)

  • FDA UDI 1450b7ab-6eef-432f-892b-254fc38a0ba2 36 fields · synced Jun 1, 2026