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Symmetry Magnafree®

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Magnafree® FDA UDI
Generic Name
Open-surgery dissector FDA UDI
Device Name
Magnafree® Dissector, Penfield, Titanium, Size 4, 8 1/4 in FDA UDI
Model / Reference
65-2405 FDA UDI
Description
Magnafree® Dissector, Penfield, Titanium, Size 4, 8 1/4 in FDA UDI

Identifiers

Primary DI / UDI-DI
00887482025581 FDA UDI
FDA Product Code
GDI FDA UDI
GMDN Term
Open-surgery dissector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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 — 8.25 Inch FDA UDI

Category: Open-surgery dissector

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

Similar devices

Also classified as Open-surgery dissector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d58d85d0-e17e-4f8e-b936-32563a7a44fe 35 fields · synced May 30, 2026