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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
Periodontal hoe FDA UDI
Device Name
PT1 HOE EN /PT2 DE # 6 HDL FDA UDI
Model / Reference
PP6691 FDA UDI
Description
PT1 HOE EN /PT2 DE # 6 HDL FDA UDI

Identifiers

Catalog Number
PP6691 FDA UDI
Primary DI / UDI-DI
10889950086640 FDA UDI
FDA Product Code
EMJ FDA UDI
GMDN Term
Periodontal hoe 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: Periodontal hoe

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 Periodontal hoe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hu-Friedy Mfg Co., Llc

Sources (1)

  • FDA UDI f91c56c1-745d-4598-9807-2569f345952c 35 fields · synced Jun 1, 2026