FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10885380180958 · Model: FMTRACH · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10885380180958
Version / Model
FMTRACH
Catalog Number
FMTRACH
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-23
Public Version
1
Public Version Date
2022-03-03
Public Version Status
New
Public Device Record Key
5d5eb8c2-edc8-4734-9c56-4c1017d5b1d5

Device Description

Silicone Non-Adhesive Foam Tracheostomy Dressing

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
NAD Dressing, wound, occlusive

GMDN Terms

Code Name
46854 Wound-nonadherent dressing, absorbent, non-antimicrobial

Identifiers

Type ID
Package 50885380180956
Package 20885380180955
Primary 10885380180958

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius