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Hemorrhoids Multiple Band Ligator Set

FDA UDI

Class II (US FDA UDI)

by Micro-Tech (Nanjing) Co., Ltd.

Identity

Trade Name
Hemorrhoids Multiple Band Ligator Set FDA UDI
Generic Name
Haemorrhoid ligation set FDA UDI
Device Name
Hemorrhoids Multiple Band Ligator Set,Applicable for endoscopic diameter(9.4~13)mm,6 ligation ring,Foreign markets,band Type:Latex FDA UDI
Model / Reference
HMBLS-6F FDA UDI
Description
Hemorrhoids Multiple Band Ligator Set,Applicable for endoscopic diameter(9.4~13)mm,6 ligation ring,Foreign markets,band Type:Latex FDA UDI

Identifiers

Primary DI / UDI-DI
06932503532037 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 220 Centimeter FDA UDI

Category: Haemorrhoid ligation set

Hemorrhoids Multiple Band Ligator Set by Micro-Tech (Nanjing) Co., 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

Sources (1)

  • FDA UDI 5bbda46f-d434-4180-84cb-eaa81088e536 35 fields · synced Jun 8, 2026