FDA UDI In Commercial Distribution 🇺🇸 United States

Celerity

DI: 10724995161597 · Model: LCB045 · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Celerity
Primary DI
10724995161597
Version / Model
LCB045
Catalog Number
LCB045
Company Name
STERIS CORPORATION
Labeler DUNS
961394798
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2019-07-02
Public Version
3
Public Version Date
2022-04-19
Public Version Status
Update
Public Device Record Key
aed11fa0-d51c-4537-a2b8-3d205abf15ab

Device Description

The Celerity 20 HP Challenge Pack is intended for qualification testing of the V-PRO Low Temperature Sterilization Systems following installation, relocation, malfunction or major repairs and for routine requalification testing.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FRC Indicator, biological sterilization process

GMDN Terms

Code Name
13732 Biological sterilization indicator

Identifiers

Type ID
Primary 10724995161597
Unit of Use 00724995161590

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K173488 000
K183294 000
K220473 000