FDA UDI In Commercial Distribution 🇺🇸 United States

CARDINAL HEALTH

DI: 10887488093789 · Model: SBA12BTHFA · CARDINAL HEALTH 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CARDINAL HEALTH
Primary DI
10887488093789
Version / Model
SBA12BTHFA
Catalog Number
SBA12BTHFA
Company Name
CARDINAL HEALTH 200, LLC
Labeler DUNS
112164780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-10
Public Version
7
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
bc2e3a28-874d-4d3b-92f6-0abc4205e62b

Device Description

STRL BOVIE TWEEZER FORCEP FFX

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 50887488093787
Primary 10887488093789

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius