← Back to catalogue

Hu-Friedy

FDA UDI

Class I (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name
HU-FRIEDY FDA UDI
Generic Name
Orthodontic metal band pusher FDA UDI
Device Name
BPS1 Band Pusher/BPS2 Band Pusher 41 Hdl FDA UDI
Model / Reference
PI6542 FDA UDI
Description
BPS1 Band Pusher/BPS2 Band Pusher 41 Hdl FDA UDI

Identifiers

Catalog Number
PI6542 FDA UDI
Primary DI / UDI-DI
10889950083205 FDA UDI
FDA Product Code
ECS FDA UDI
GMDN Term
Orthodontic metal band pusher 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: Orthodontic metal band pusher

Hu-Friedy by Hu-Friedy Mfg Co., Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic metal band pusher.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d41c802f-c898-4320-bc55-b5707b76f687 35 fields · synced May 31, 2026