FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00818834028356 · Model: 301-12218 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00818834028356
Version / Model
301-12218
Catalog Number
301-12218
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-30
Public Version
2
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
c808a2f0-1f31-4740-bd9c-c72e755c19b3

Device Description

VibraPEP Valved Tee Adapter

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CAI Circuit, breathing (w connector, adaptor, y piece)

GMDN Terms

Code Name
61346 Straight/elbow breathing circuit connector, single-use

Identifiers

Type ID
Package 00818834028370
Package 00818834028363
Primary 00818834028356