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Monarch Disposable Anoscope

FDA UDI

Class II (US FDA UDI)

by Monarch Molding, Inc.

Identity

Trade Name
MONARCH DISPOSABLE ANOSCOPE FDA UDI
Generic Name
Haemorrhoid electrotherapy system procedure kit FDA UDI
Device Name
ONE TIME USE 18mm x 90mm (CLEAR) PLASTIC DISPOSABLE ANOSCOPE 100/EACH PER CASE-2/BAGS OF 50 EACH FDA UDI
Model / Reference
1890C FDA UDI
Description
ONE TIME USE 18mm x 90mm (CLEAR) PLASTIC DISPOSABLE ANOSCOPE 100/EACH PER CASE-2/BAGS OF 50 EACH FDA UDI

Identifiers

Catalog Number
1890C FDA UDI
Primary DI / UDI-DI
00613970018908 FDA UDI
FDA Product Code
KDM FDA UDI
GMDN Term
Haemorrhoid electrotherapy system procedure kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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: Haemorrhoid electrotherapy system procedure kit

Monarch Disposable Anoscope by Monarch Molding, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemorrhoid electrotherapy system procedure kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Monarch Molding, Inc.

Sources (1)

  • FDA UDI a0315b0f-2e75-4388-af2b-9a2843594128 35 fields · synced May 30, 2026