FDA UDI In Commercial Distribution 🇺🇸 United States

Corning

DI: H108230121 · Model: 23012 · Corning Incorporated
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Corning
Primary DI
H108230121
Version / Model
23012
Catalog Number
23012
Company Name
Corning Incorporated
Labeler DUNS
001307735
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-09
Public Version
1
Public Version Date
2025-01-17
Public Version Status
New
Public Device Record Key
b5363453-8c27-49d4-98d9-3c9e5b672700

Device Description

Corning HYPERStack 12-Layer Cell Culture Vessel, CellBIND Treated, Dual filters, ASQ accessory, Sterile, 1 per bag, 4 per case

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KJA Flask, tissue culture

GMDN Terms

Code Name
44904 Blood/tissue storage/culture container

Identifiers

Type ID
Package H108230123
Primary H108230121

Customer Contacts