FDA UDI In Commercial Distribution 🇺🇸 United States

Instaform

DI: 00628341930321 · Model: 1 · CDR Systems Inc
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Instaform
Primary DI
00628341930321
Version / Model
1
Catalog Number
IFF03
Company Name
CDR Systems Inc
Labeler DUNS
206950904
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-31
Public Version
2
Public Version Date
2020-01-16
Public Version Status
Update
Public Device Record Key
32666661-0faa-460e-9517-a11996e9c999

Device Description

Instaform Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
IYE Accelerator, Linear, Medical

GMDN Terms

Code Name
40894 Patient positioning foam mould kit

Identifiers

Type ID
Package 10628341930328
Primary 00628341930321
Package 30628341930322
Package 20628341930325

Customer Contacts

Phone
403-850-7035

Premarket Submissions

Submission Number Supplement Number
K122888 000