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Next Gen Driver

FDA UDI

Class I (US FDA UDI)

by Bioaccess Inc

Identity

Trade Name
Next Gen Driver FDA UDI
Generic Name
Bone/joint surgical power tool motorized handpiece/set, electric, single-use FDA UDI
Model / Reference
NGD1000 FDA UDI

Identifiers

Primary DI / UDI-DI
M791NGD10000 FDA UDI
FDA Product Code
GFF FDA UDI
GMDN Term
Bone/joint surgical power tool motorized handpiece/set, electric, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

No

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: Bone/joint surgical power tool motorized handpiece/set, electric, single-use

Next Gen Driver by Bioaccess Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone/joint surgical power tool motorized handpiece/set, electric, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bioaccess Inc

Sources (1)

  • FDA UDI 7930e25a-604e-4b21-8d8f-fbb83610fc91 32 fields · synced Jun 1, 2026