← Back to catalogue

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, 65 mL FDA UDI
Model / Reference
204820 FDA UDI
Description
Pump Reservoir for WalkMed Infusion Pump, 65 mL FDA UDI

Identifiers

Catalog Number
IPR-86 FDA UDI
Primary DI / UDI-DI
00859695006046 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 — 65 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

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

Manufacturer

Sources (1)

  • FDA UDI 9beee4cb-6b7a-4271-a0d7-8f16fffe2d57 37 fields · synced Jun 8, 2026