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ShortShot

FDA UDI

Class II (US FDA UDI)

by Cook Ireland, Ltd.

Identity

Trade Name
ShortShot FDA UDI
Generic Name
Haemorrhoid ligation set FDA UDI
Device Name
Shortshot Saeed Hemorrhoidal Multi-Band Ligator With Triview Anoscope FDA UDI
Model / Reference
G34181 FDA UDI
Description
Shortshot Saeed Hemorrhoidal Multi-Band Ligator With Triview Anoscope FDA UDI

Identifiers

Catalog Number
C-HMBL-4-TRI FDA UDI
Primary DI / UDI-DI
00827002341814 FDA UDI
FDA Product Code
FHN FDA UDI
GMDN Term
Haemorrhoid ligation set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4400 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Haemorrhoid ligation set

ShortShot by Cook Ireland, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemorrhoid ligation set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Ireland, Ltd.

Sources (1)

  • FDA UDI 7d605f7a-daa8-4b3e-92fb-de208806d713 36 fields · synced May 30, 2026