FDA UDI In Commercial Distribution 🇺🇸 United States

Filter Assembly

DI: 10850082007186 · Model: 21003 · ARMM INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Filter Assembly
Primary DI
10850082007186
Version / Model
21003
Company Name
ARMM INC.
Labeler DUNS
797391778
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2023-06-08
Public Version
1
Public Version Date
2023-06-16
Public Version Status
New
Public Device Record Key
c06469d9-3b2e-4e41-8fee-197a1f583a28

Device Description

Filter Assembly - 1'

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HIF Insufflator, Laparoscopic

GMDN Terms

Code Name
60738 Endoscopic insufflation tubing set, single-use

Identifiers

Type ID
Unit of Use 00850082007189
Primary 10850082007186

Customer Contacts

Phone
7148488190