← Back to catalogue

Bur Cranial Spiral 25mm St

FDA UDI

Class II (US FDA UDI)

by Bien-Air Surgery SA

Identity

Trade Name
Bur Cranial Spiral 25mm St FDA UDI
Generic Name
Cranial bur, single-use FDA UDI
Model / Reference
1100413 FDA UDI

Identifiers

Catalog Number
1100413-001 FDA UDI
Primary DI / UDI-DI
17630055503708 FDA UDI
510(k) Number
K173066 FDA UDI
FDA Product Code
HBC FDA UDI
HBE FDA UDI
GMDN Term
Cranial bur, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4360 FDA UDI
882.4310 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cranial bur, single-use

Bur Cranial Spiral 25mm St by Bien-Air Surgery SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cranial bur, single-use.

Cleared under the same submission

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
Bien-Air Surgery SA

Sources (1)

  • FDA UDI ecc7061a-40dc-4cff-b630-00fcbd26c529 34 fields · synced May 30, 2026