Pemco Inc

FDA UDI

Class II (US FDA UDI)

by Pemco, Inc.

Identity

Trade Name: PEMCO INC FDA UDI
Generic Name: Suction cannula, reusable FDA UDI
Device Name: Intracardiac Sucker, Pediatric Round Handle at 30 Degree Angle has 3/8" barbed end. Works with the following tips Tips 1450-15 6.4mm diameter, 1450-16 4.0mm diameter, 1450-17 2.0mm diameter, & 1450-17L 2.0mm diameter (long) FDA UDI
Model / Reference: 1450JR-01 FDA UDI
Description: Intracardiac Sucker, Pediatric Round Handle at 30 Degree Angle has 3/8" barbed end. Works with the following tips Tips 1450-15 6.4mm diameter, 1450-16 4.0mm diameter, 1450-17 2.0mm diameter, & 1450-17L 2.0mm diameter (long) FDA UDI

Identifiers

Catalog Number: 1450JR-01 FDA UDI
Primary DI / UDI-DI: B1521450JR010 FDA UDI
FDA Product Code: DTS FDA UDI
GMDN Term: Suction cannula, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.4420 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

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 7 Inch FDA UDI

Category: Suction cannula, reusable

Pemco Inc by Pemco, Inc. — 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: Pemco, Inc.

Sources (1)

FDA UDI ee1488f4-e962-401f-9f0b-a5094a1f5c2a 36 fields · synced May 30, 2026