FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00815277020510 · Model: 2160-20500 · BOUND TREE MEDICAL, LLC
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00815277020510
Version / Model
2160-20500
Catalog Number
2160-20500
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-14
Public Version
3
Public Version Date
2022-08-16
Public Version Status
Update
Public Device Record Key
b98c7e35-d297-4906-a7dd-904c3309bae5

Device Description

Curaplex Deployable Chest tube Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
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
GAR Suture, nonabsorbable, synthetic, polyamide
KDQ BOTTLE, COLLECTION, VACUUM
PLY antimicrobial drapes

GMDN Terms

Code Name
47200 Pneumothorax catheter insertion set

Identifiers

Type ID
Primary 00815277020510
Package 00810094570026