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Stiegmann-Goff

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
STIEGMANN-GOFF FDA UDI
Generic Name
Oesophageal endoscopic ligator, single-use FDA UDI
Device Name
STIEGMANN-GOFF ENDOSCOPIC LIGATOR FDA UDI
Model / Reference
200220 FDA UDI
Description
STIEGMANN-GOFF ENDOSCOPIC LIGATOR FDA UDI

Identifiers

Catalog Number
200220 FDA UDI
Primary DI / UDI-DI
10653405053637 FDA UDI
FDA Product Code
FHN FDA UDI
GMDN Term
Oesophageal endoscopic ligator, single-use 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Oesophageal endoscopic ligator, single-use

Stiegmann-Goff by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oesophageal endoscopic ligator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 2f1bf7b5-8e90-4433-b1d0-70f9d49f50b1 35 fields · synced May 30, 2026