FDA UDI In Commercial Distribution 🇺🇸 United States

Corning

DI: H108119151 · Model: 11915 · Corning Incorporated
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Corning
Primary DI
H108119151
Version / Model
11915
Catalog Number
11915
Company Name
Corning Incorporated
Labeler DUNS
001307735
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-02
Public Version
4
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
f6369493-6328-4348-b36b-cdc1a94ab0cf

Device Description

Corning 3L DSF with 2 Aseptic Transfer Caps: Cap1 tubing, connectors; Cap 2, Port1: barb lock, air filter; Port2: silicone tubing, Y-connector, connectors, assembled, Sterile, 2 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
No
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
KJE SPINNER SYSTEM, CELL CULTURE

GMDN Terms

Code Name
44904 Blood/tissue storage/culture container

Identifiers

Type ID
Package H108119153
Primary H108119151

Customer Contacts