Symmetry Surgical

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name: Symmetry Surgical FDA UDI
Generic Name: Gastro-urological guidewire, reusable FDA UDI
Device Name: Symmetry® Director, Grooved, 6 1/4 in, 158 mm FDA UDI
Model / Reference: 09-1516 FDA UDI
Description: Symmetry® Director, Grooved, 6 1/4 in, 158 mm FDA UDI

Identifiers

Catalog Number: 09-1516 FDA UDI
Primary DI / UDI-DI: 00887482053171 FDA UDI
FDA Product Code: MDM FDA UDI
GMDN Term: Gastro-urological guidewire, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 6.25 Inch FDA UDI

Category: Gastro-urological guidewire, reusable

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

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Ambler Surgical — Ambler Surgical, LLC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Symmetry Surgical Inc.

Sources (1)

FDA UDI 3185497b-4fac-42ed-a742-f56d5f8469ea 36 fields · synced May 30, 2026