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Pashley Frazier Suction

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
PASHLEY FRAZIER SUCTION FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
Device Name
PASHLEY FRAZIER SUCTION CURVED RIGHT FDA UDI
Model / Reference
1463-501 FDA UDI
Description
PASHLEY FRAZIER SUCTION CURVED RIGHT FDA UDI

Identifiers

Primary DI / UDI-DI
B09914635010 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI

Pashley Frazier Suction by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fb0331e3-34b3-4d7a-abbe-74a38a8224e8 35 fields · synced Jun 1, 2026