FDA UDI Not in Commercial Distribution 🇺🇸 United States

Decompression Tube

DI: 00842071104115 · Model: E3-1834 · APPLIED MEDICAL TECHNOLOGY, INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Decompression Tube
Primary DI
00842071104115
Version / Model
E3-1834
Catalog Number
E3-1834, 3-1834
Company Name
APPLIED MEDICAL TECHNOLOGY, INC.
Labeler DUNS
038101861
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-31
Public Version
5
Public Version Date
2023-07-03
Public Version Status
Update
Public Device Record Key
d65091f2-6596-429b-8da7-7d697ed29de7
Distribution End Date
2023-06-30

Device Description

18F x 3.4 cm Decompression Tube (Pouched)

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
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
No
Sterilization Prior Use
No

Product Codes

Code Name
KGC Tube, Gastro-Enterostomy
KNT Tubes, Gastrointestinal (And Accessories)

GMDN Terms

Code Name
35419 Gastrostomy tube

Identifiers

Type ID
Package 00842071106256
Primary 00842071104115

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 18 French
Length 3.4 Centimeter