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Symmetry Freer

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Freer FDA UDI
Generic Name
Cartilage knife FDA UDI
Device Name
Symmetry® Knife, Freer Septum, Angled, 7 in FDA UDI
Model / Reference
66-5208 FDA UDI
Description
Symmetry® Knife, Freer Septum, Angled, 7 in FDA UDI

Identifiers

Catalog Number
66-5208 FDA UDI
Primary DI / UDI-DI
00887482119860 FDA UDI
FDA Product Code
KTG FDA UDI
GMDN Term
Cartilage knife 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 — 7 Inch FDA UDI

Category: Cartilage knife

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

Similar devices

Also classified as Cartilage knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 142da558-0a54-4e06-9b81-0764e15b997c 36 fields · synced May 30, 2026