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Symmetry Dittel

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Dittel FDA UDI
Generic Name
Uterine sound, reusable FDA UDI
Device Name
Symmetry® Sound, Dittel Urethral, Curved, 18 Fr FDA UDI
Model / Reference
51-6218 FDA UDI
Description
Symmetry® Sound, Dittel Urethral, Curved, 18 Fr FDA UDI

Identifiers

Catalog Number
51-6218 FDA UDI
Primary DI / UDI-DI
00887482075616 FDA UDI
FDA Product Code
FBX FDA UDI
GMDN Term
Uterine sound, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5520 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 — 18 French FDA UDI

Category: Uterine sound, reusable

Symmetry Dittel by Symmetry Surgical Inc. — Class I — 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 6e9f1178-af63-483c-a69b-98f6fb787ef1 36 fields · synced Jun 8, 2026