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Plasdent

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
Plasdent FDA UDI
Generic Name
Root canal irrigation blunt needle FDA UDI
Device Name
Bent Needle Tips - 22 Gauge, Grey FDA UDI
Model / Reference
BNT-22 FDA UDI
Description
Bent Needle Tips - 22 Gauge, Grey FDA UDI

Identifiers

Catalog Number
BNT-22 FDA UDI
Primary DI / UDI-DI
D832BNT221 FDA UDI
FDA Product Code
DZM FDA UDI
GMDN Term
Root canal irrigation blunt needle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Category: Root canal irrigation blunt needle

Plasdent by Plasdent Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Root canal irrigation blunt needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI c1d2b911-b792-4487-809f-a648d5577a56 34 fields · synced May 30, 2026