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Symmetry Shea

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Shea FDA UDI
Generic Name
Middle ear file/rasp FDA UDI
Device Name
Symmetry® Searcher, Shea Forward, 45 FDA UDI
Model / Reference
62-0475 FDA UDI
Description
Symmetry® Searcher, Shea Forward, 45 FDA UDI

Identifiers

Primary DI / UDI-DI
00887482116548 FDA UDI
FDA Product Code
JZC FDA UDI
GMDN Term
Middle ear file/rasp 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
Angle — 45 degree FDA UDI

Category: Middle ear file/rasp

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

Similar devices

Also classified as Middle ear file/rasp.

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 2e1b2a8f-51d8-4e22-bb43-25ece44cecba 35 fields · synced May 30, 2026