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Paul Banditt

FDA UDI

Class I (US FDA UDI)

by Terlain Enterprises, Inc.

Identity

Trade Name
Paul Banditt FDA UDI
Generic Name
Wire holding/twisting pliers FDA UDI
Device Name
BANDITT TOE NAIL CLIPPER 3312 13.5CM FDA UDI
Model / Reference
TNC3312 FDA UDI
Description
BANDITT TOE NAIL CLIPPER 3312 13.5CM FDA UDI

Identifiers

Primary DI / UDI-DI
D955TNC33121 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Wire holding/twisting pliers FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Wire holding/twisting pliers

Paul Banditt by Terlain Enterprises, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire holding/twisting pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terlain Enterprises, Inc.

Sources (1)

  • FDA UDI 4274471e-54f2-4353-9d8f-542e1853c609 33 fields · synced May 30, 2026