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Cranio Guard 25mm fix

FDA UDI

Class II (US FDA UDI)

by Bien-Air Surgery SA

Identity

Trade Name
Cranio Guard 25mm fix FDA UDI
Generic Name
Trephining power tool attachment FDA UDI
Model / Reference
1600887 FDA UDI

Identifiers

Catalog Number
1600887-001 FDA UDI
Primary DI / UDI-DI
J00716008870011 FDA UDI
FDA Product Code
HBC FDA UDI
GMDN Term
Trephining power tool attachment FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4360 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Cranio Guard 25mm fix by Bien-Air Surgery SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 04c10798-9c6f-4a8a-bfa0-0f134bd5b6b1 34 fields · synced Jun 8, 2026