← Back to catalogue

Beeline motIV

FDA UDI

Class II (US FDA UDI)

by Rex Pj Tech LLC

Identity

Trade Name
Beeline motIV FDA UDI
Generic Name
Prefilled mechanical infusion pump/catheter FDA UDI
Device Name
Infusion Set (0.8 ml/hr) FDA UDI
Model / Reference
BL1D00/8 FDA UDI
Description
Infusion Set (0.8 ml/hr) FDA UDI

Identifiers

Primary DI / UDI-DI
00857362007037 FDA UDI
FDA Product Code
FRN FDA UDI
GMDN Term
Prefilled mechanical infusion pump/catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Prefilled mechanical infusion pump/catheter

Beeline motIV by Rex Pj Tech LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Prefilled mechanical infusion pump/catheter.

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
Rex Pj Tech LLC

Sources (1)

  • FDA UDI ef6c21d7-1d24-4822-ac80-a9a6afa64751 33 fields · synced May 30, 2026