← Back to catalogue

3M™ RelyX™

FDA UDI

Class I (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
3M™ RelyX™ FDA UDI
Generic Name
Steel dental bur, reusable FDA UDI
Device Name
3M™ RelyX™ Fiber Post Drill, 56864, Yellow, Size 1 FDA UDI
Model / Reference
56864 FDA UDI
Description
3M™ RelyX™ Fiber Post Drill, 56864, Yellow, Size 1 FDA UDI

Identifiers

Catalog Number
56864 FDA UDI
Primary DI / UDI-DI
04035077010153 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Steel dental bur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 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

Yes

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

Category: Steel dental bur, reusable

3M™ RelyX™ by 3M Deutschland GmbH — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
3M Deutschland GmbH

Sources (1)

  • FDA UDI c249bbe2-cd90-4a01-a4c3-1e2e7e999e4b 35 fields · synced Jun 1, 2026