← Back to catalogue

Corning® PureCoat™

FDA UDI

Class I (US FDA UDI)

by Corning Incorporated

Identity

Trade Name
Corning® PureCoat™ FDA UDI
Generic Name
Blood/tissue storage/culture container FDA UDI
Device Name
Collagen I Peptide 24 Well Clear Plate, with Lid, Sterile, 5/Pack, 10/Case FDA UDI
Model / Reference
356271 FDA UDI
Description
Collagen I Peptide 24 Well Clear Plate, with Lid, Sterile, 5/Pack, 10/Case FDA UDI

Identifiers

Catalog Number
356271 FDA UDI
Primary DI / UDI-DI
20389151000447 FDA UDI
FDA Product Code
KIZ 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood/tissue storage/culture container

Corning® PureCoat™ 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

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

Manufacturer

Sources (1)

  • FDA UDI 9d441402-841e-4669-9066-85f8d1a070aa 35 fields · synced Jun 6, 2026