FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00812277037968 · Model: 301-FO-MAC-2-S · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00812277037968
Version / Model
301-FO-MAC-2-S
Catalog Number
301-FO-MAC-2-S
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-30
Public Version
1
Public Version Date
2023-01-09
Public Version Status
New
Public Device Record Key
1d8eb98a-f32a-446d-a052-59578bf60e62

Device Description

MAC 2,STANDARD,DISP.,CURAVIEW FO,GREEN SYSTEM,COMBO

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
CCW LARYNGOSCOPE, RIGID

GMDN Terms

Code Name
62918 Rigid intubation laryngoscope, single-use

Identifiers

Type ID
Package 00810071630118
Package 00812277039221
Primary 00812277037968