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3/16" x 1/4" Neonate Pack

FDA UDI

Class II (US FDA UDI)

by Datascope Corp.

Identity

Trade Name
3/16" x 1/4" Neonate Pack FDA UDI
Generic Name
Cardiopulmonary bypass system blood tubing set FDA UDI
Device Name
Stainless Steel Cooling coil BC 60 plus CDI Sat Cell 1/4" System 100 Gas Filter Temperature Probe FDA UDI
Model / Reference
BO-T 46200 FDA UDI
Description
Stainless Steel Cooling coil BC 60 plus CDI Sat Cell 1/4" System 100 Gas Filter Temperature Probe FDA UDI

Identifiers

Catalog Number
701065620 FDA UDI
Primary DI / UDI-DI
00607567208063 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Cardiopulmonary bypass system blood tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4210 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

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

3/16" x 1/4" Neonate 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 361a3e8c-2a76-4bf9-9a46-68d14aacd6e1 37 fields · synced May 30, 2026