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Symmetry Frazier

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Frazier FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
Device Name
Symmetry® Suction Tube, Frazier, Medium Angle, 7 Fr, 4 1/4 in, 108 mm FDA UDI
Model / Reference
09-8307 FDA UDI
Description
Symmetry® Suction Tube, Frazier, Medium Angle, 7 Fr, 4 1/4 in, 108 mm FDA UDI

Identifiers

Catalog Number
09-8307 FDA UDI
Primary DI / UDI-DI
00887482047699 FDA UDI
FDA Product Code
JZF FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 4.25 Inch FDA UDI
Catheter Gauge — 7 French FDA UDI

Category: Surgical/emergency suction cannula, non-illuminating, reusable

Symmetry Frazier by Symmetry Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ea9c1237-29d3-47e0-97bb-1ec327069823 36 fields · synced May 30, 2026