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Topsuper Med

FDA UDI

Class II (US FDA UDI)

by Topsuper Med, Inc.

Identity

Trade Name
Topsuper Med FDA UDI
Generic Name
Haemorrhoid ligation set FDA UDI
Model / Reference
TPYZC-3 FDA UDI

Identifiers

Primary DI / UDI-DI
00197644720941 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Haemorrhoid ligation set

Topsuper Med by Topsuper Med, Inc. — 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
Topsuper Med, Inc.

Sources (1)

  • FDA UDI c0893bd0-8128-41eb-9bc2-00587d1d1882 32 fields · synced Jun 6, 2026