← Back to catalogue

Symmetry Baron

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Baron FDA UDI
Generic Name
Tracheostomy tube obturator FDA UDI
Device Name
Symmetry® Wire; Baron Obturator (Stylet); 7 Fr FDA UDI
Model / Reference
62-2220S FDA UDI
Description
Symmetry® Wire; Baron Obturator (Stylet); 7 Fr FDA UDI

Identifiers

Catalog Number
62-2220S FDA UDI
Primary DI / UDI-DI
00887482116746 FDA UDI
FDA Product Code
JZF FDA UDI
GMDN Term
Tracheostomy tube obturator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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
Catheter Gauge — 7 French FDA UDI

Category: Tracheostomy tube obturator

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

Similar devices

Also classified as Tracheostomy tube obturator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI 17137211-c096-4a2e-8e16-072388d02b48 36 fields · synced May 29, 2026