FDA UDI In Commercial Distribution 🇺🇸 United States

TIDI

DI: 00618125131013 · Model: 20991 · TIDI PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TIDI
Primary DI
00618125131013
Version / Model
20991
Catalog Number
97901590
Company Name
TIDI PRODUCTS, LLC
Labeler DUNS
063519193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-07
Public Version
1
Public Version Date
2022-10-17
Public Version Status
New
Public Device Record Key
5d48091e-3f17-4064-93db-da456fd1e37c

Device Description

Camera Covers, Fits C-U2 HD Camera

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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KQM Camera, Surgical And Accessories

GMDN Terms

Code Name
12535 Medical equipment drape, single-use

Identifiers

Type ID
Package 10618125131010
Primary 00618125131013