FDA UDI In Commercial Distribution 🇺🇸 United States

Sterimed

DI: 00867878000484 · Model: 3692 · STERIMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Sterimed
Primary DI
00867878000484
Version / Model
3692
Company Name
STERIMED LLC
Labeler DUNS
080284658
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-05
Public Version
3
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
f9423058-6aa6-4ef2-932f-17ac9979776d

Device Description

Equipment Cover 36" X 92" W/Tape (3692)

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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
["Radiation Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
IZI System, X-Ray, Angiographic

GMDN Terms

Code Name
12535 Medical equipment drape, single-use

Identifiers

Type ID
Primary 00867878000484
Package 10867878000481
Package 20867878000488

Customer Contacts

Phone
770-387-0771

Premarket Submissions

Submission Number Supplement Number
K853044 000