← Back to catalogue

Hirschman Rectal Speculum

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
HIRSCHMAN RECTAL SPECULUM FDA UDI
Generic Name
Rectal speculum FDA UDI
Device Name
HIRSCHMAN RECTAL SPECULUM LARGE TUBE FDA UDI
Model / Reference
508-366 FDA UDI
Description
HIRSCHMAN RECTAL SPECULUM LARGE TUBE FDA UDI

Identifiers

Catalog Number
508-366 FDA UDI
Primary DI / UDI-DI
00192896087880 FDA UDI
FDA Product Code
FFQ FDA UDI
GMDN Term
Rectal speculum FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

Category: Rectal speculum

Hirschman Rectal Speculum by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rectal speculum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 5cf6c4b6-be31-416b-a876-8b8338d4a9e0 36 fields · synced May 30, 2026