← Back to catalogue

Neoview

FDA UDI

Class I (US FDA UDI)

by In2bones

Identity

Trade Name
NEOVIEW FDA UDI
Generic Name
Fluted surgical drill bit, reusable FDA UDI
Model / Reference
P03 00051 FDA UDI

Identifiers

Catalog Number
P03 00051 FDA UDI
Primary DI / UDI-DI
03760225715789 FDA UDI
FDA Product Code
GFG FDA UDI
GMDN Term
Fluted surgical drill bit, reusable 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fluted surgical drill bit, reusable

Neoview by In2bones — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, 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
In2bones

Sources (1)

  • FDA UDI b46b1604-d915-4249-9d34-9b8cf623ef7f 34 fields · synced May 30, 2026