FDA UDI In Commercial Distribution 🇺🇸 United States

Epi-Max™ Epistaxis Procedure Pack

DI: 14063107101424 · Model: 60-402 · Boston Medical Products, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Epi-Max™ Epistaxis Procedure Pack
Primary DI
14063107101424
Version / Model
60-402
Catalog Number
60-402
Company Name
Boston Medical Products, Inc.
Labeler DUNS
131855157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-29
Public Version
2
Public Version Date
2023-02-20
Public Version Status
Update
Public Device Record Key
df4a2eb1-45d1-4fc1-ac77-459a9f7f32b9

Device Description

Size: 97 mm Length; Type: Anterior/Posterior

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
Yes
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
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
No

Product Codes

Code Name
EMX Balloon, Epistaxis

GMDN Terms

Code Name
12699 Nasal haemostatic balloon

Identifiers

Type ID
Package 34063107101428
Primary 14063107101424

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K972076 000

Device Sizes

Type Value Unit Text
Length 97 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight