Symmetry Castroviejo

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name: Symmetry Castroviejo FDA UDI
Generic Name: Common bile duct dilator FDA UDI
Device Name: Symmetry® Dilator, Castroviejo Lacrimal, Double-Ended FDA UDI
Model / Reference: 60-1991 FDA UDI
Description: Symmetry® Dilator, Castroviejo Lacrimal, Double-Ended FDA UDI

Identifiers

Catalog Number: 60-1991 FDA UDI
Primary DI / UDI-DI: 00887482041093 FDA UDI
FDA Product Code: HNW FDA UDI
GMDN Term: Common bile duct dilator FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4350 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

Category: Common bile duct dilator

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

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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 487743f2-8164-420f-b406-c5b0ae6878a6 35 fields · synced May 31, 2026