← Back to catalogue

Symmetry Darrach

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Darrach FDA UDI
Generic Name
Bone lever/elevator, reusable FDA UDI
Device Name
Symmetry® Elevator, Darrach, 16mm Blade Width; Blunt; 19 mm Jaw; 10 1/4 in; 260 mm FDA UDI
Model / Reference
77-6003 FDA UDI
Description
Symmetry® Elevator, Darrach, 16mm Blade Width; Blunt; 19 mm Jaw; 10 1/4 in; 260 mm FDA UDI

Identifiers

Catalog Number
77-6003 FDA UDI
Primary DI / UDI-DI
00887482126080 FDA UDI
FDA Product Code
GEG FDA UDI
GMDN Term
Bone lever/elevator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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 — 10.25 Inch FDA UDI
Width — 16 Millimeter FDA UDI

Category: Bone lever/elevator, reusable

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

Similar devices

Also classified as Bone lever/elevator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3c070a79-f5dd-41e7-9a87-0ec95e065eb5 36 fields · synced May 30, 2026