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Symmetry Frazier

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Frazier FDA UDI
Generic Name
Brain spatula FDA UDI
Device Name
Symmetry® Spatula; Frazier Dura; 2.0mm / 3.0mm wide; 6 in FDA UDI
Model / Reference
57-3505 FDA UDI
Description
Symmetry® Spatula; Frazier Dura; 2.0mm / 3.0mm wide; 6 in FDA UDI

Identifiers

Catalog Number
57-3505 FDA UDI
Primary DI / UDI-DI
00887482039007 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Brain spatula 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 — 6 Inch FDA UDI
Width — 2 Millimeter FDA UDI
Width — 3 Millimeter FDA UDI

Category: Brain spatula

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

Similar devices

Also classified as Brain spatula.

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 d47b5032-69cc-4e44-9d46-8fe99b858e81 36 fields · synced May 31, 2026