FDA UDI Not in Commercial Distribution 🇺🇸 United States

CODMAN

DI: 10886704043829 · Model: AP-09150 · Cerenovus, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CODMAN
Primary DI
10886704043829
Version / Model
AP-09150
Catalog Number
AP09150
Company Name
Cerenovus, Inc.
Labeler DUNS
607846297
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-20
Public Version
5
Public Version Date
2023-09-15
Public Version Status
Update
Public Device Record Key
1ef14a30-64d0-470c-b7a6-6541d7f7e785
Distribution End Date
2021-12-31

Device Description

3000 Series High Temperature Drape for use with CODMAN O.R. Heater AP-09100

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LKK PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

GMDN Terms

Code Name
34071 Implantable intrathecal infusion pump, nonprogrammable

Identifiers

Type ID
Package 20886704043826
Primary 10886704043829

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P890055 012
P890055 017
P890055 021
P890055 023
P890055 027

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-20 – 40 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
-20 – 40 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Do not use if opened or damaged.