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Bonopty Adapter

FDA UDI

Class I (US FDA UDI)

by Apriomed AB

Identity

Trade Name
Bonopty Adapter FDA UDI
Generic Name
Surgical instrument handle grip FDA UDI
Device Name
Universal connector compatible with AprioMed Bonopty drills. FDA UDI
Model / Reference
250 FDA UDI
Description
Universal connector compatible with AprioMed Bonopty drills. FDA UDI

Identifiers

Catalog Number
250 FDA UDI
Primary DI / UDI-DI
07350031352504 FDA UDI
FDA Product Code
HXY FDA UDI
GMDN Term
Surgical instrument handle grip FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Surgical instrument handle grip

Bonopty Adapter by Apriomed AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle grip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Apriomed AB

Sources (1)

  • FDA UDI 63e2909d-7dc8-4af9-b235-e2499d913f44 36 fields · synced May 30, 2026