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Peak Medical

FDA UDI

Class II (US FDA UDI)

by PEAK MEDICAL Distribution Inc

Identity

Trade Name
PEAK MEDICAL FDA UDI
Generic Name
In-line backflow valve, single-use FDA UDI
Device Name
Stopcock with male luer lock and 6 mm diameter barb fitting FDA UDI
Model / Reference
335200-32 FDA UDI
Description
Stopcock with male luer lock and 6 mm diameter barb fitting FDA UDI

Identifiers

Primary DI / UDI-DI
G4533352000320 FDA UDI
FDA Product Code
FMG FDA UDI
GMDN Term
In-line backflow valve, single-use 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

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: In-line backflow valve, single-use

Peak Medical by PEAK MEDICAL Distribution Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as In-line backflow valve, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PEAK MEDICAL Distribution Inc

Sources (1)

  • FDA UDI 3051ce4e-771e-45c8-8497-9f1b048419d4 33 fields · synced May 30, 2026