FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617028255 · Model: 6700139-KIT · BOUND TREE MEDICAL, LLC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Curaplex
Primary DI
00817617028255
Version / Model
6700139-KIT
Catalog Number
6700139-KIT
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-18
Public Version
3
Public Version Date
2022-08-16
Public Version Status
Update
Public Device Record Key
b631ac3a-448a-4c66-bd42-962c1a91a9e9

Device Description

Curaplex *Custom* PHI Surgical Cricothyrotomy 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
No
Not Made with NRL
No
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
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days
KDQ BOTTLE, COLLECTION, VACUUM

GMDN Terms

Code Name
45926 Cricothyrotomy kit, single-use

Identifiers

Type ID
Primary 00817617028255
Package 00810094570576