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LA Childrens ECC Pack

FDA UDI

Class II (US FDA UDI)

by Datascope Corp.

Identity

Trade Name
LA Childrens ECC Pack FDA UDI
Generic Name
Cardiopulmonary bypass system blood tubing set FDA UDI
Device Name
701050970 BEQ-HMOD 30000-USA Pediatric Quadrox iD 701054444 Better Bladder 1/4 700000111 Blood Microfilter System SQ 40 S 701031084 Prebypass filter w/o Vent Porous Media 3/8x3/8 701045515 Pediatric Temp Probe FDA UDI
Model / Reference
BEQ-TOP 49100 FDA UDI
Description
701050970 BEQ-HMOD 30000-USA Pediatric Quadrox iD 701054444 Better Bladder 1/4 700000111 Blood Microfilter System SQ 40 S 701031084 Prebypass filter w/o Vent Porous Media 3/8x3/8 701045515 Pediatric Temp Probe FDA UDI

Identifiers

Catalog Number
701066976 FDA UDI
Primary DI / UDI-DI
00607567206403 FDA UDI
FDA Product Code
DWE FDA UDI
GMDN Term
Cardiopulmonary bypass system blood tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4390 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

LA Childrens ECC Pack by Datascope Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Datascope Corp.

Sources (1)

  • FDA UDI df1a8342-ed7b-41a0-b8ca-42798a33134b 37 fields · synced May 31, 2026