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Symmetry Bailey

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Bailey FDA UDI
Generic Name
Vessel approximator FDA UDI
Device Name
Symmetry® Approximator, Bailey Rib, Pediatric, 6 5/8 in FDA UDI
Model / Reference
54-2530 FDA UDI
Description
Symmetry® Approximator, Bailey Rib, Pediatric, 6 5/8 in FDA UDI

Identifiers

Catalog Number
54-2530 FDA UDI
Primary DI / UDI-DI
00887482079584 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

Dimensions & Sizes

Size
Length — 6.625 Inch FDA UDI

Category: Vessel approximator

Symmetry Bailey 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 6d85683b-e9ca-4575-95e2-8d6dfef7eb66 36 fields · synced Jun 8, 2026