← Back to catalogue

Pd-Cttu-600504

FDA UDI

Class I (US FDA UDI)

by Nakanishi Inc.

Identity

Trade Name
PD-CTTU-600504 FDA UDI
Generic Name
Luminal device flushing tubing set, reusable FDA UDI
Model / Reference
PD-CTTU-600504 FDA UDI

Identifiers

Primary DI / UDI-DI
04589551354573 FDA UDI
510(k) Number
K202120 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Luminal device flushing tubing set, 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Luminal device flushing tubing set, reusable

Pd-Cttu-600504 by Nakanishi Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luminal device flushing tubing set, reusable.

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 62cb8046-63e9-4da1-835f-a90b58aef88d 33 fields · synced May 31, 2026