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Symmetry Bailey-Gibbon

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Bailey-Gibbon FDA UDI
Generic Name
Vessel approximator FDA UDI
Device Name
Symmetry® Approximator, Bailey-Gibbon Rib FDA UDI
Model / Reference
50-8055 FDA UDI
Description
Symmetry® Approximator, Bailey-Gibbon Rib FDA UDI

Identifiers

Catalog Number
50-8055 FDA UDI
Primary DI / UDI-DI
00887482019931 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Vessel approximator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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

Category: Vessel approximator

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

Similar devices

Also classified as Vessel approximator.

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 168a8e5b-cdd8-489e-b1c0-7dd391cdb968 35 fields · synced May 30, 2026