← Back to catalogue

Robotic, Drill Bit Dia 3 mm, Lg. 220 mm

FDA UDI

Class II (US FDA UDI)

by Ecential Robotics

Identity

Trade Name
Robotic, Drill Bit Dia 3 mm, Lg. 220 mm FDA UDI
Generic Name
Fluted surgical drill bit, reusable FDA UDI
Model / Reference
A40001 FDA UDI

Identifiers

Primary DI / UDI-DI
03701311500193 FDA UDI
510(k) Number
K221028 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Fluted surgical drill bit, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI

Robotic, Drill Bit Dia 3 mm, Lg. 220 mm by Ecential Robotics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

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
Ecential Robotics

Sources (1)

  • FDA UDI a22a74d1-26a7-45fa-b92a-f4176f55d40f 35 fields · synced May 30, 2026