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Hu-Friedy

FDA UDI

Class I (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name
HU-FRIEDY FDA UDI
Generic Name
Endodontic plugger FDA UDI
Device Name
PLUGGER DE #41 HANDLE FDA UDI
Model / Reference
MCB7160 FDA UDI
Description
PLUGGER DE #41 HANDLE FDA UDI

Identifiers

Catalog Number
MCB7160 FDA UDI
Primary DI / UDI-DI
10889950080006 FDA UDI
FDA Product Code
EKR FDA UDI
GMDN Term
Endodontic plugger 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endodontic plugger

The Endodontic Plugger, a handheld, manually-operated dental instrument specifically designed to compress filling materials in root canals. Mainly axial direction, with a cylindrical or tapered, circular cross-section and flat-tipped end.

Similar devices

Also classified as Endodontic plugger.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 349b69c9-7695-4d98-8578-286009fd12c6 35 fields · synced Jun 29, 2026