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Statcorp

FDA UDI

Class I (US FDA UDI)

by Statcorp Medical

Identity

Trade Name
STATCORP FDA UDI
Generic Name
Intravenous pressure infusor, manual, reusable FDA UDI
Device Name
UNIFUSOR+,REUSABLE,3000ML,ANEROID,THUMBWHEEL,EA FDA UDI
Model / Reference
STATCORP FDA UDI
Description
UNIFUSOR+,REUSABLE,3000ML,ANEROID,THUMBWHEEL,EA FDA UDI

Identifiers

Catalog Number
1105FGA FDA UDI
Primary DI / UDI-DI
10841522127847 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

Yes

FDA UDI

Category: Intravenous pressure infusor, manual, reusable

Statcorp by Statcorp Medical — 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
Statcorp Medical

Sources (1)

  • FDA UDI 0bb7efde-7be2-47cf-83b2-1d30477636f7 35 fields · synced Jun 1, 2026