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E-Z Draw

FDA UDI

Class I (US FDA UDI)

by Reprocessing Products Corp

Identity

Trade Name
E-Z Draw FDA UDI
Generic Name
Haemodialysis treatment kit FDA UDI
Device Name
Sample Port FDA UDI
Model / Reference
D300-2012 FDA UDI
Description
Sample Port FDA UDI

Identifiers

Primary DI / UDI-DI
00858293006359 FDA UDI
FDA Product Code
MON FDA UDI
GMDN Term
Haemodialysis treatment kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5820 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haemodialysis treatment kit

E-Z Draw by Reprocessing Products Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis treatment kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reprocessing Products Corp

Sources (1)

  • FDA UDI e9b650ec-4a86-4eca-a3b1-4ecfa00da768 33 fields · synced May 30, 2026