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Symmetry RUSKIN

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry RUSKIN FDA UDI
Generic Name
Spinal rongeur FDA UDI
Device Name
Symmetry® Rongeur; Ruskin; Straight; Small Jaw FDA UDI
Model / Reference
53-1310 FDA UDI
Description
Symmetry® Rongeur; Ruskin; Straight; Small Jaw FDA UDI

Identifiers

Catalog Number
53-1310 FDA UDI
Primary DI / UDI-DI
00887482022382 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Spinal rongeur FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4840 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

Category: Spinal rongeur

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

Similar devices

Also classified as Spinal rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI 084b0492-d8f1-4c7f-8c79-f8e4510db782 35 fields · synced May 30, 2026