← Back to catalogue

PM PERFO + Cable

FDA UDI

Class II (US FDA UDI)

by Bien-Air Surgery SA

Identity

Trade Name
PM PERFO + Cable FDA UDI
Generic Name
Manual cranial rotary handpiece, reusable FDA UDI
Model / Reference
1700500 FDA UDI

Identifiers

Catalog Number
1700500-001 FDA UDI
Primary DI / UDI-DI
17630055506136 FDA UDI
FDA Product Code
HBC FDA UDI
HBE FDA UDI
GMDN Term
Manual cranial rotary handpiece, reusable 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

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

Yes

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

Category: Manual cranial rotary handpiece, reusable

PM PERFO + Cable by Bien-Air Surgery SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual cranial rotary handpiece, 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
Bien-Air Surgery SA

Sources (1)

  • FDA UDI c8552a59-cfce-45e0-8325-75f6cb8c0ba1 33 fields · synced Jun 6, 2026