FDA UDI In Commercial Distribution 🇺🇸 United States

Insufflation Tubing

DI: 10850082007179 · Model: 21101 · ARMM INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Insufflation Tubing
Primary DI
10850082007179
Version / Model
21101
Company Name
ARMM INC.
Labeler DUNS
797391778
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-12-22
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
ef225a02-6bf0-413e-9d1c-b3fe18743864

Device Description

Insufflation Tubing - 8' / Rotating Male Luers

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
Primary 10850082007179
Unit of Use 00850082007172

Customer Contacts

Phone
7148488190