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Slf-001-Vp

FDA UDI

Class I (US FDA UDI)

by GNI Co., Ltd

Identity

Trade Name
SLF-001-VP FDA UDI
Generic Name
Self-ligating orthodontic bracket open/close tool FDA UDI
Model / Reference
SLF-001-VP FDA UDI

Identifiers

Primary DI / UDI-DI
08800046046466 FDA UDI
FDA Product Code
ECP FDA UDI
GMDN Term
Self-ligating orthodontic bracket open/close tool 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: Self-ligating orthodontic bracket open/close tool

Slf-001-Vp by GNI Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-ligating orthodontic bracket open/close tool.

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 b1825c3a-cf13-4043-a2c9-b7245e712c79 32 fields · synced May 30, 2026