FDA UDI In Commercial Distribution 🇺🇸 United States

BodyMed

DI: 00815991024689 · Model: BDMSBS10 · BOXOUT, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BodyMed
Primary DI
00815991024689
Version / Model
BDMSBS10
Company Name
BOXOUT, LLC
Labeler DUNS
066689993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-05
Public Version
1
Public Version Date
2022-12-13
Public Version Status
New
Public Device Record Key
cc2b725a-311e-4106-b228-1dfec7f5bc1c

Device Description

Stainless Steel Surgical Blade Size 10,100 pcs/box

Device Characteristics

Single Use
Yes
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
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
GFA Blade, Saw, General & Plastic Surgery, Surgical

GMDN Terms

Code Name
37445 Manual scalpel blade, single-use

Identifiers

Type ID
Primary 00815991024689
Package 20815991024683