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P01-01

FDA UDI

Class I (US FDA UDI)

by GNI Co., Ltd

Identity

Trade Name
P01-01 FDA UDI
Generic Name
Orthodontic pliers FDA UDI
Model / Reference
P01-01 FDA UDI

Identifiers

Primary DI / UDI-DI
08800046045896 FDA UDI
FDA Product Code
JEX FDA UDI
GMDN Term
Orthodontic pliers FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthodontic pliers

P01-01 by GNI Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
GNI Co., Ltd

Sources (1)

  • FDA UDI 1f0fc660-3c56-4e11-b2f7-45254860a8e7 32 fields · synced May 30, 2026