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WalkMed®

FDA UDI

Class I (US FDA UDI)

by WalkMed Technologies, LLC

Identity

Trade Name
WalkMed® FDA UDI
Generic Name
Parenteral/enteral solution bag FDA UDI
Device Name
Pump Reservoir for WalkMed Infusion Pump, 250 mL FDA UDI
Model / Reference
204822 FDA UDI
Description
Pump Reservoir for WalkMed Infusion Pump, 250 mL FDA UDI

Identifiers

Catalog Number
IPR-250 FDA UDI
Primary DI / UDI-DI
00859695006060 FDA UDI
FDA Product Code
BTC FDA UDI
GMDN Term
Parenteral/enteral solution bag FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5320 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

Dimensions & Sizes

Size
Total Volume — 250 Milliliter FDA UDI

Category: Parenteral/enteral solution bag

WalkMed® by WalkMed Technologies, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Parenteral/enteral solution bag.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5c0fb2cd-8157-4f4a-974a-22f2c9ddaa97 37 fields · synced May 30, 2026