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Symmetry Russel-Davis

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Russel-Davis FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Symmetry® Blade; Russel-Davis Tongue; 18 mm Wide; 57 mm Long FDA UDI
Model / Reference
45-5330 FDA UDI
Description
Symmetry® Blade; Russel-Davis Tongue; 18 mm Wide; 57 mm Long FDA UDI

Identifiers

Catalog Number
45-5330 FDA UDI
Primary DI / UDI-DI
00887482073827 FDA UDI
FDA Product Code
KBL FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable 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
Width — 18 Millimeter FDA UDI
Length — 57 Millimeter FDA UDI

Category: Surgical retractor/retraction system blade, reusable

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

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

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 37c550e3-0056-4692-bcc6-a9c997f361c1 36 fields · synced Jun 6, 2026