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Bondent

FDA UDI

Class I (US FDA UDI)

by United Dental Changzhou

Identity

Trade Name
Bondent FDA UDI
Generic Name
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI
Model / Reference
UDG-Platinum V.EU FDA UDI

Identifiers

Primary DI / UDI-DI
06942135200969 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rotary/reciprocating endodontic file/rasp, reusable

Bondent by United Dental Changzhou — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rotary/reciprocating endodontic file/rasp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 70a44a92-d370-4393-93fc-848e73c3f2d4 32 fields · synced May 29, 2026