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Stp Lb Gxl Bls Rad

FDA UDI

Class II (US FDA UDI)

by Elecam Medical Agricultural Cooperative Society Ltd.

Identity

Trade Name
STP LB GXL BLS RAD FDA UDI
Generic Name
Stopcock FDA UDI
Device Name
D600 Discofix ® High– Flow 4-Way Stopcock FDA UDI
Model / Reference
Large Bore Stopcock FDA UDI
Description
D600 Discofix ® High– Flow 4-Way Stopcock FDA UDI

Identifiers

Catalog Number
456061 FDA UDI
Primary DI / UDI-DI
07290102590049 FDA UDI
510(k) Number
K022895 FDA UDI
K190489 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
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 — 200 KiloPascal FDA UDI

Category: Stopcock

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

Similar devices

Also classified as Stopcock.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d4524aec-9718-4a34-8061-a30195c0e218 38 fields · synced Jun 8, 2026