← Back to catalogue

Hu-Friedy MFG Co., LLC.

FDA UDI

Class I (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name
Hu-Friedy MFG Co., LLC. FDA UDI
Generic Name
Periodontal curette FDA UDI
Device Name
#5/6 After5 Langer Curette Res Lav Smth FDA UDI
Model / Reference
SL5/6AFC8M FDA UDI
Description
#5/6 After5 Langer Curette Res Lav Smth FDA UDI

Identifiers

Primary DI / UDI-DI
10889950096564 FDA UDI
FDA Product Code
EMS FDA UDI
GMDN Term
Periodontal curette FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
Not 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

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

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 78f0945b-59ef-493f-b9f1-285ac170abaa 35 fields · synced May 31, 2026