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Greenwald Surgical Company, Inc.

FDA UDI

Class I (US FDA UDI)

by Grace Manufacturing Inc

Identity

Trade Name
Greenwald Surgical Company, Inc. FDA UDI
Generic Name
Urethral sound, reusable FDA UDI
Device Name
Hodgson Sound, Straight, Pediatric. Short taper for periodic dilation after urethrotomy. Mirror finish, stainless steel, precision machined. FDA UDI
Model / Reference
58050-08 FDA UDI
Description
Hodgson Sound, Straight, Pediatric. Short taper for periodic dilation after urethrotomy. Mirror finish, stainless steel, precision machined. FDA UDI

Identifiers

Catalog Number
U338 FDA UDI
Primary DI / UDI-DI
10801334012199 FDA UDI
FDA Product Code
FBX FDA UDI
GMDN Term
Urethral 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 5 Inch FDA UDI
Catheter Gauge — 8 French FDA UDI

Category: Urethral sound, reusable

Greenwald Surgical Company, Inc. by Grace Manufacturing Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urethral sound, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 30ba8c82-12b9-4038-8bec-baf04cc1ab4f 35 fields · synced May 30, 2026