FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex®

DI: 00810094578381 · Model: 8600-01521 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Curaplex®
Primary DI
00810094578381
Version / Model
8600-01521
Catalog Number
8600-01521
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-09
Public Version
1
Public Version Date
2025-07-17
Public Version Status
New
Public Device Record Key
4698d091-10ab-4ba8-88d2-57b9d60e8d8e

Device Description

*Custom* THS CCMC Resus Kit, Pediatric

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
BTM Ventilator, emergency, manual (resuscitator)

GMDN Terms

Code Name
36086 Pulmonary resuscitator, manual, single-use

Identifiers

Type ID
Primary 00810094578381