FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00810094576240 · Model: 2141-13510 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00810094576240
Version / Model
2141-13510
Catalog Number
2141-13510
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-30
Public Version
1
Public Version Date
2023-10-09
Public Version Status
New
Public Device Record Key
f051d9ca-cd11-42ed-9ba1-853fa3ad3207

Device Description

Curaplex Select Laryngoscope Handle, Reusable, LED, Water-Resistant 96ea/bx

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
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
CCW LARYNGOSCOPE, RIGID

GMDN Terms

Code Name
15076 Rigid intubation laryngoscope, reusable

Identifiers

Type ID
Package 00810094576264
Primary 00810094576240
Package 00810094576257