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Symmetry Garrett

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Garrett FDA UDI
Generic Name
Common bile duct dilator FDA UDI
Device Name
Symmetry® Dilator, Garrett, Malleable, 5 1/2 in, 139 mm, (Set of 9) FDA UDI
Model / Reference
55-7002 FDA UDI
Description
Symmetry® Dilator, Garrett, Malleable, 5 1/2 in, 139 mm, (Set of 9) FDA UDI

Identifiers

Catalog Number
55-7002 FDA UDI
Primary DI / UDI-DI
00887482160893 FDA UDI
FDA Product Code
DWP FDA UDI
GMDN Term
Common bile duct dilator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4475 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 — 5.5 Inch FDA UDI

Category: Common bile duct dilator

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

Similar devices

Also classified as Common bile duct dilator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a068a49e-39fe-4313-bd19-e9157de92a3c 36 fields · synced May 30, 2026