FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00812277030211 · Model: 5590 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
25

Basic Information

Brand Name
Curaplex
Primary DI
00812277030211
Version / Model
5590
Catalog Number
1212-12110
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
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
f7a28df1-9f16-46e6-b215-90723e7c6e5d

Device Description

Curaplex Abdominal Combine Dressing, Sterile, 5" x 9", 25/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 00812277030334
Package 00812277034097
Primary 00812277030211
Unit of Use 00812277034073