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InfuseIT

FDA UDI

Class I (US FDA UDI)

by Salter Labs

Identity

Trade Name
InfuseIT FDA UDI
Generic Name
Intravenous pressure infusor, manual, reusable FDA UDI
Device Name
InfuselT 1000ml Disposable Pressure Infusor FDA UDI
Model / Reference
ZIT-1002 FDA UDI
Description
InfuselT 1000ml Disposable Pressure Infusor FDA UDI

Identifiers

Catalog Number
ZIT-1002 FDA UDI
Primary DI / UDI-DI
00607411915369 FDA UDI
FDA Product Code
KZD FDA UDI
GMDN Term
Intravenous pressure infusor, manual, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5420 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 1000 Milliliter FDA UDI

Category: Intravenous pressure infusor, manual, reusable

InfuseIT by Salter Labs — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous pressure infusor, manual, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Salter Labs

Sources (1)

  • FDA UDI 311f9adb-b5b8-4622-b1d1-441073db3d9e 36 fields · synced May 30, 2026