← Back to catalogue

Stp 4way Rad

FDA UDI

Class II (US FDA UDI)

by Elecam Medical Agricultural Cooperative Society Ltd.

Identity

Trade Name
STP 4WAY RAD FDA UDI
Generic Name
Stopcock FDA UDI
Device Name
STP 4WAY RAD FDA UDI
Model / Reference
NA FDA UDI
Description
STP 4WAY RAD FDA UDI

Identifiers

Catalog Number
572488 FDA UDI
Primary DI / UDI-DI
07290102590025 FDA UDI
510(k) Number
K022895 FDA UDI
FDA Product Code
FMG FDA UDI
GMDN Term
Stopcock FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Pressure — 300 KiloPascal FDA UDI

Stp 4way Rad by Elecam Medical Agricultural Cooperative Society Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

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

Sources (1)

  • FDA UDI 2b4bb96d-7680-4466-96b3-2cda6bdc3b30 39 fields · synced Jun 6, 2026