Jedmed

FDA UDI

Class II (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name: JEDMED FDA UDI
Generic Name: Suction system bottle FDA UDI
Device Name: Conversion Kit /Glass Trap FDA UDI
Model / Reference: 03-5555 FDA UDI
Description: Conversion Kit /Glass Trap FDA UDI

Identifiers

Catalog Number: 03-5555 FDA UDI
Primary DI / UDI-DI: M6330355550 FDA UDI
FDA Product Code: KDQ FDA UDI
GMDN Term: Suction system bottle FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6740 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Suction system bottle

Jedmed by JEDMED Instrument Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: JEDMED Instrument Company

Sources (1)

FDA UDI 11bf0128-38e0-4bf1-9de1-f4f8bf651d79 35 fields · synced May 30, 2026