← Back to catalogue

E-Z Draw Sample Port

FDA UDI

Class I (US FDA UDI)

by Reprocessing Products Corp

Identity

Trade Name
E-Z Draw Sample Port FDA UDI
Generic Name
Haemodialysis treatment kit FDA UDI
Device Name
D300-2011 E-Z Draw Sample Port FDA UDI
Model / Reference
D300-2011 FDA UDI
Description
D300-2011 E-Z Draw Sample Port FDA UDI

Identifiers

Primary DI / UDI-DI
00858293006847 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 Sample Port 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Reprocessing Products Corp

Sources (1)

  • FDA UDI f18e5b78-5150-4170-b8d6-b0f235554893 33 fields · synced May 31, 2026