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Symmetry Kahn

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Kahn FDA UDI
Generic Name
Uterine sound, reusable FDA UDI
Device Name
Tip; PTFE Tips For Kahn Cannula 52-0842 FDA UDI
Model / Reference
52-0800 FDA UDI
Description
Tip; PTFE Tips For Kahn Cannula 52-0842 FDA UDI

Identifiers

Catalog Number
52-0800 FDA UDI
Primary DI / UDI-DI
00887482141533 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Uterine sound, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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: Uterine sound, reusable

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

Similar devices

Also classified as Uterine sound, reusable.

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 334ce9a2-1dec-48ac-b80d-f54fbb5663f6 35 fields · synced May 30, 2026