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Nordent Manufacturing Inc

FDA UDI

Class I (US FDA UDI)

by Nordent Manufacturing Inc

Identity

Trade Name
NORDENT MANUFACTURING INC FDA UDI
Generic Name
Periodontal file/rasp, manual FDA UDI
Device Name
FILE PERIOD.,DE, SUGARMAN 3-4, FDA UDI
Model / Reference
CEFPS3-4 FDA UDI
Description
FILE PERIOD.,DE, SUGARMAN 3-4, FDA UDI

Identifiers

Primary DI / UDI-DI
00840018645509 FDA UDI
FDA Product Code
EMR FDA UDI
GMDN Term
Periodontal file/rasp, manual 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

Yes

FDA UDI

Category: Periodontal file/rasp, manual

NORDENT MANUFACTURING INC's Periodontal File/Rasp, Manual is a high-quality dental instrument designed to scrape and smooth during periodontal procedures. This one-piece instrument features various forms of ridged cutting surfaces at its working end(s), available in different sizes and designs.

Similar devices

Also classified as Periodontal file/rasp, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 77713fad-6401-4cb3-b681-5e11adbd0848 33 fields · synced Jul 23, 2026