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Compass Microsaw G2

FDA UDI

Class I (US FDA UDI)

by Bien-Air Surgery SA

Identity

Trade Name
Compass Microsaw G2 FDA UDI
Generic Name
Sawing power tool attachment, reciprocating FDA UDI
Model / Reference
1600658 FDA UDI

Identifiers

Primary DI / UDI-DI
07630055505613 FDA UDI
FDA Product Code
DWI FDA UDI
GMDN Term
Sawing power tool attachment, reciprocating FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Compass Microsaw G2 by Bien-Air Surgery SA — Class I — 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 09a45a6f-6239-422c-b37e-e4e3ef3a5c6d 33 fields · synced May 30, 2026