FDA UDI In Commercial Distribution 🇺🇸 United States

BALLARD™

DI: 10889483563311 · Model: 12254 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

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Basic Information

Brand Name
BALLARD™
Primary DI
10889483563311
Version / Model
12254
Catalog Number
12254
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-12
Public Version
1
Public Version Date
2026-01-20
Public Version Status
New
Public Device Record Key
1e3e789e-6e58-4a9d-abb8-a6b2c39c4372

Device Description

BALLARD™ ORAL CARE SWAB, Individually Wrapped with 15 cm Plastic Handle

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
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 20889483563318
Primary 10889483563311
Package 30889483563315
Previous 00609038968803

Customer Contacts