← Back to catalogue

NSK Sterile Burs/Drills

FDA UDI

Class II (US FDA UDI)

by Nakanishi Inc.

Identity

Trade Name
NSK Sterile Burs/Drills FDA UDI
Generic Name
Orthopaedic bur, single-use FDA UDI
Model / Reference
PDS-2CBM-20 FDA UDI

Identifiers

Primary DI / UDI-DI
04560264545847 FDA UDI
510(k) Number
K132264 FDA UDI
FDA Product Code
HBC FDA UDI
GMDN Term
Orthopaedic bur, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4360 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic bur, single-use

NSK Sterile Burs/Drills by Nakanishi Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bur, single-use.

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
Nakanishi Inc.

Sources (1)

  • FDA UDI 51f878c8-6633-4418-97f1-b8e985636da2 34 fields · synced Jun 8, 2026