← Back to catalogue

Symmetry Hardy™

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Hardy™ FDA UDI
Generic Name
Open-surgery dissector FDA UDI
Device Name
Symmetry® Enucleator, Hardy Transphenoid, Standard Right, Bayonet, 9 1/2 in FDA UDI
Model / Reference
58-7560 FDA UDI
Description
Symmetry® Enucleator, Hardy Transphenoid, Standard Right, Bayonet, 9 1/2 in FDA UDI

Identifiers

Catalog Number
58-7560 FDA UDI
Primary DI / UDI-DI
00887482104453 FDA UDI
FDA Product Code
GZX FDA UDI
GMDN Term
Open-surgery dissector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4525 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 — 9.5 Inch FDA UDI

Category: Open-surgery dissector

Symmetry Hardy™ 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI ea3965b1-584e-489c-9ceb-14bdb946bbcb 36 fields · synced Jun 8, 2026