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Primado2

FDA UDI

Class I (US FDA UDI)

by Nakanishi Inc.

Identity

Trade Name
Primado2 FDA UDI
Generic Name
Surgical instrument maintenance lubricant FDA UDI
Model / Reference
P200-EZ-SM FDA UDI

Identifiers

Primary DI / UDI-DI
04589551356430 FDA UDI
510(k) Number
K163483 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Surgical instrument maintenance lubricant FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical instrument maintenance lubricant

Primado2 by Nakanishi Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument maintenance lubricant.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nakanishi Inc.

Sources (1)

  • FDA UDI a5e6bc14-e421-47f2-9941-652477cdc50d 33 fields · synced May 30, 2026