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Corning

FDA UDI

Class I (US FDA UDI)

by Corning Incorporated

Identity

Trade Name
Corning FDA UDI
Generic Name
Blood/tissue storage/culture container FDA UDI
Device Name
Corning Cellstack-10, CellBIND treated, barb cap to 3" 3/8", to 12" 3/32, WYE connector to 2x 18" 2x Luer Connector, Right side vent cap FDA UDI
Model / Reference
11857 FDA UDI
Description
Corning Cellstack-10, CellBIND treated, barb cap to 3" 3/8", to 12" 3/32, WYE connector to 2x 18" 2x Luer Connector, Right side vent cap FDA UDI

Identifiers

Catalog Number
11857 FDA UDI
Primary DI / UDI-DI
H108118571 FDA UDI
FDA Product Code
KJA FDA UDI
GMDN Term
Blood/tissue storage/culture container FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.2240 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood/tissue storage/culture container

Corning by Corning Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood/tissue storage/culture container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 173ee929-edaa-4f2d-8a5c-fa6517fe4e14 35 fields · synced Jun 1, 2026