FDA UDI In Commercial Distribution 🇺🇸 United States

Sterimed

DI: 00850341007653 · Model: 0136B · STERIMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Sterimed
Primary DI
00850341007653
Version / Model
0136B
Company Name
STERIMED LLC
Labeler DUNS
080284658
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
3
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
9acb655a-7c1e-4678-9504-28c10364835b

Device Description

Band Bag 36" X 36", Non-Sterile

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
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Radiation Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
IZI System, X-Ray, Angiographic

GMDN Terms

Code Name
43071 X-ray system cover

Identifiers

Type ID
Package 10850341007650
Primary 00850341007653

Customer Contacts

Phone
770-387-0771

Premarket Submissions

Submission Number Supplement Number
K853044 000