FDA UDI In Commercial Distribution 🇺🇸 United States

Sterimed

DI: 00860001790214 · Model: 3520SB · STERIMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Sterimed
Primary DI
00860001790214
Version / Model
3520SB
Company Name
STERIMED LLC
Labeler DUNS
080284658
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-27
Public Version
2
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
7497a96c-7986-42d2-81a3-15681ed27310

Device Description

Equipment Drape - 35" X 20" 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
["Ethylene Oxide", "Radiation Sterilization"]

Product Codes

Code Name
IZI System, X-Ray, Angiographic

GMDN Terms

Code Name
12535 Medical equipment drape, single-use

Identifiers

Type ID
Package 10860001790211
Primary 00860001790214

Customer Contacts

Phone
770-387-0771

Premarket Submissions

Submission Number Supplement Number
K853044 000