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Pilling

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Haemorrhoid ligator FDA UDI
Device Name
GASKETS FOR HEMORRIDAL LATEX LIGATOR FDA UDI
Model / Reference
IPN911954 FDA UDI
Description
GASKETS FOR HEMORRIDAL LATEX LIGATOR FDA UDI

Identifiers

Catalog Number
P16404 FDA UDI
Primary DI / UDI-DI
34026704651604 FDA UDI
FDA Product Code
FHN FDA UDI
GMDN Term
Haemorrhoid ligator 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Haemorrhoid ligator

Pilling by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemorrhoid ligator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 1638f524-ad1e-498a-9b47-ca6add650b42 35 fields · synced Jun 8, 2026