FDA UDI In Commercial Distribution 🇺🇸 United States

K303

DI: 00197513003236 · Model: RLK303-3XF · BURLINGTON MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K303
Primary DI
00197513003236
Version / Model
RLK303-3XF
Company Name
BURLINGTON MEDICAL, LLC
Labeler DUNS
083381202
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-09
Public Version
1
Public Version Date
2023-02-17
Public Version Status
New
Public Device Record Key
d164482c-768b-427e-9862-6c739ea30cf1

Device Description

Custom: K303 Full Overlap Wrap Around Kilt .5mm Lead Size Three Extra Large Female

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EAJ Apron, Leaded

GMDN Terms

Code Name
38355 Radiation shielding apron

Identifiers

Type ID
Primary 00197513003236