FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00812277036336 · Model: KLTSD404K-DOD · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00812277036336
Version / Model
KLTSD404K-DOD
Catalog Number
KLTSD404K-DOD
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-30
Public Version
1
Public Version Date
2020-05-08
Public Version Status
New
Public Device Record Key
270cc6d9-d6e5-4816-b942-fdc27d9e7426

Device Description

Airway Kit, Supraglottic W/Et Holder, size 4

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
No
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
CAE AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY

GMDN Terms

Code Name
45036 Laryngeal mask airway, single-use

Identifiers

Type ID
Primary 00812277036336