FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 05030267064151 · Model: 2310000 · Intersurgical Incorporated
Product Codes
0
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
05030267064151
Version / Model
2310000
Company Name
Intersurgical Incorporated
Labeler DUNS
785952607
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-15
Public Version
2
Public Version Date
2022-02-07
Public Version Status
Update
Public Device Record Key
896406bd-4c67-4069-b9a9-0c007a6aa133

Device Description

DUAL FLOAT AUTO FILL HUMIDIFICATION CHAMBER WITH FILL SET

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

GMDN Terms

Code Name
60699 Inspiratory line humidification chamber, single-use

Identifiers

Type ID
Package 05030267037773
Primary 05030267064151

Customer Contacts

Phone
3154512900