FDA UDI In Commercial Distribution 🇺🇸 United States

OEC

DI: 00618125152179 · Model: 31883 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
OEC
Primary DI
00618125152179
Version / Model
31883
Catalog Number
31883
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-26
Public Version
3
Public Version Date
2023-07-28
Public Version Status
Update
Public Device Record Key
08d10c42-6c9a-4594-8921-ab0992254b1f

Device Description

R15/KIT, SS/PP C-ARM DRAPE W/F

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PUI Drape, Surgical, Exempt

GMDN Terms

Code Name
12535 Medical equipment drape, single-use

Identifiers

Type ID
Primary 00618125152179
Previous 01618125152178
Package 10618125152176