FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00812277030181 · Model: 1212-12107 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
2

Basic Information

Brand Name
Curaplex
Primary DI
00812277030181
Version / Model
1212-12107
Catalog Number
1212-12107
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2018-12-15
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
f0796722-9e7e-47b2-8207-289f5341a1c7

Device Description

Curaplex Sterile, Sponge, non Woven 4 Ply, 2" x 2" 2/PK 50PK/BX

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48134 Woven gauze pad

Identifiers

Type ID
Package 00812277030303
Primary 00812277030181
Package 00812277030396
Unit of Use 00812277034042