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Symmetry Hegar

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Hegar FDA UDI
Generic Name
Urethral dilator, reusable FDA UDI
Device Name
Symmetry® Dilator, Hegar Uterine, Set of 8, 7 3/4 in, 197 mm FDA UDI
Model / Reference
25-5536 FDA UDI
Description
Symmetry® Dilator, Hegar Uterine, Set of 8, 7 3/4 in, 197 mm FDA UDI

Identifiers

Catalog Number
25-5536 FDA UDI
Primary DI / UDI-DI
00887482002438 FDA UDI
FDA Product Code
HDQ FDA UDI
GMDN Term
Urethral dilator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4530 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 — 7.75 Inch FDA UDI

Category: Urethral dilator, reusable

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

Similar devices

Also classified as Urethral dilator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fe43f4d6-2412-407d-a8a8-dec8c469b121 36 fields · synced May 30, 2026