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Burkhart Dental

FDA UDI

Class I (US FDA UDI)

by Nordent Manufacturing Inc

Identity

Trade Name
BURKHART DENTAL FDA UDI
Generic Name
Dental surgical scissors FDA UDI
Device Name
BDS SCISS #320 DEAN ANG.CURV 7" PREM FDA UDI
Model / Reference
S320/BH FDA UDI
Description
BDS SCISS #320 DEAN ANG.CURV 7" PREM FDA UDI

Identifiers

Primary DI / UDI-DI
00840018604353 FDA UDI
FDA Product Code
EGN FDA UDI
GMDN Term
Dental surgical scissors 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: Dental surgical scissors

Burkhart Dental by Nordent Manufacturing Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 06fe1794-eca5-4f29-8a40-3abb41082d81 33 fields · synced Jun 8, 2026