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Symmetry Tyding

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Tyding FDA UDI
Generic Name
Tonsil snare FDA UDI
Device Name
Symmetry® Snare, Tyding Tonsil, 9 1/2 in FDA UDI
Model / Reference
72-5051 FDA UDI
Description
Symmetry® Snare, Tyding Tonsil, 9 1/2 in FDA UDI

Identifiers

Catalog Number
72-5051 FDA UDI
Primary DI / UDI-DI
00887482122914 FDA UDI
FDA Product Code
KBZ FDA UDI
GMDN Term
Tonsil snare 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
Length — 9.5 Inch FDA UDI

Category: Tonsil snare

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

Similar devices

Also classified as Tonsil snare.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1142d8b6-6ba5-42c3-84fd-0a658ca35f38 36 fields · synced Jun 8, 2026