← 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
Interproximal dental gauge, reusable FDA UDI
Device Name
1.2MM Chafer Reduction Gauge FDA UDI
Model / Reference
CRG7131 FDA UDI
Description
1.2MM Chafer Reduction Gauge FDA UDI

Identifiers

Catalog Number
CRG7131 FDA UDI
Primary DI / UDI-DI
10889950045036 FDA UDI
FDA Product Code
EIL FDA UDI
GMDN Term
Interproximal dental gauge, reusable 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: Interproximal dental gauge, reusable

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 Interproximal dental gauge, reusable.

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 faf796c3-ca0a-478b-b829-2596b9bd2b34 35 fields · synced May 31, 2026