FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00810071634291 · Model: 1121-36567 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Curaplex
Primary DI
00810071634291
Version / Model
1121-36567
Catalog Number
1121-36567
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-30
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
b12ba858-5b4f-4122-a79a-8ba268cf18fd

Device Description

Curaplex Rolled Gauze Bandage, Non-Sterile 3in 12rl/bg, 8bg/cs

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
No
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48127 Woven gauze roll/sheet

Identifiers

Type ID
Package 00810094575199
Primary 00810071634291
Package 00810071634949