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RA L Ø2.35x26 Lindemann

FDA UDI

Class I (US FDA UDI)

by Bien-Air Surgery SA

Identity

Trade Name
RA L Ø2.35x26 Lindemann FDA UDI
Generic Name
Steel dental bur, single-use FDA UDI
Model / Reference
1100867 FDA UDI

Identifiers

Catalog Number
1100867-001 FDA UDI
Primary DI / UDI-DI
17630055517125 FDA UDI
FDA Product Code
GFF FDA UDI
GMDN Term
Steel dental bur, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Steel dental bur, single-use

RA L Ø2.35x26 Lindemann by Bien-Air Surgery SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Steel dental bur, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bien-Air Surgery SA

Sources (1)

  • FDA UDI b2293a47-cf3b-4bad-b097-32aec0565f59 33 fields · synced May 29, 2026