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Dentech

FDA UDI

Class I (US FDA UDI)

by Dentech Corp.

Identity

Trade Name
DENTECH FDA UDI
Generic Name
Steel dental bur, reusable FDA UDI
Model / Reference
30014711 FDA UDI

Identifiers

Primary DI / UDI-DI
04560218680167 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Steel dental bur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3240 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: Steel dental bur, reusable

Dentech by Dentech Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Steel dental bur, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentech Corp.

Sources (1)

  • FDA UDI 1f083e26-79f0-4670-a976-0f40b74e3128 32 fields · synced Jun 8, 2026