FDA UDI In Commercial Distribution 🇺🇸 United States

BALLARD™

DI: 10889483565537 · Model: 12249 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
5
Pkg Device Count
20

Basic Information

Brand Name
BALLARD™
Primary DI
10889483565537
Version / Model
12249
Catalog Number
12249
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2025-11-17
Public Version
2
Public Version Date
2026-01-16
Public Version Status
Update
Public Device Record Key
67c0a0ea-4196-48f6-afc8-dfe2be4426ea

Device Description

BALLARD™ ORAL CARE SWAB, Bulk Packed

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KXF Applicator, Absorbent Tipped, Non-Sterile

GMDN Terms

Code Name
45172 Oral care kit, single-use

Identifiers

Type ID
Package 30889483565531
Primary 10889483565537
Package 20889483565534
Previous 00609038968766
Unit of Use 00889483565530

Customer Contacts