FDA UDI In Commercial Distribution 🇺🇸 United States

LANTOR CUBE BOWIE DICK TEST PACK

DI: 10732224710140 · Model: LCR-025 · SPS Medical Supply Corp.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LANTOR CUBE BOWIE DICK TEST PACK
Primary DI
10732224710140
Version / Model
LCR-025
Catalog Number
LCR-025
Company Name
SPS Medical Supply Corp.
Labeler DUNS
194877072
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-15
Public Version
5
Public Version Date
2023-08-31
Public Version Status
Update
Public Device Record Key
7e2d51a1-ca9b-4e35-b12c-df3c4b48f436

Device Description

Reusable Bowie-Dick Test Pack for testing the efficacy of prevacuum sterilizers.

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
JOJ Indicator, physical/chemical sterilization process

GMDN Terms

Code Name
35362 Chemical/physical sterilization process indicator

Identifiers

Type ID
Package 50732224710148
Primary 10732224710140

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Controlled room temperature per USP