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Symmetry Hardy™

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Hardy™ FDA UDI
Generic Name
Scalpel handle, reusable FDA UDI
Device Name
Symmetry® Knife Handle, Hardy Transsphenoidal Instrument, Lateral, 9 1/2 in, 241 mm FDA UDI
Model / Reference
58-7579 FDA UDI
Description
Symmetry® Knife Handle, Hardy Transsphenoidal Instrument, Lateral, 9 1/2 in, 241 mm FDA UDI

Identifiers

Catalog Number
58-7579 FDA UDI
Primary DI / UDI-DI
00887482104521 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Scalpel handle, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4535 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: Scalpel handle, reusable

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

Similar devices

Also classified as Scalpel handle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fa88acd4-d115-4286-aa57-793f8558afdb 36 fields · synced Jun 1, 2026