FDA UDI In Commercial Distribution 🇺🇸 United States

STERIMED, Inc.

DI: 00815588025945 · Model: 1010260I3030VA · STERIMED INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
STERIMED, Inc.
Primary DI
00815588025945
Version / Model
1010260I3030VA
Catalog Number
1010260I3030VA
Company Name
STERIMED INC.
Labeler DUNS
182052670
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2021-10-26
Public Version
1
Public Version Date
2021-11-03
Public Version Status
New
Public Device Record Key
0628ca71-180f-4f4e-bd39-00d748088eef

Device Description

Sterisheet RF 60I 30 x 30

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
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
FRG Wrap, Sterilization

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Unit of Use 00815588025938
Primary 00815588025945

Premarket Submissions

Submission Number Supplement Number
K931202 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry