FDA UDI Not in Commercial Distribution 🇺🇸 United States

Inoject Kit

DI: 05707480105861 · Model: 744-US/SET · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Inoject Kit
Primary DI
05707480105861
Version / Model
744-US/SET
Catalog Number
744-US/SET
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
3
Public Version Date
2018-06-11
Public Version Status
Update
Public Device Record Key
1dc9afe1-1151-4397-8452-4239a22b6e66
Distribution End Date
2017-11-02

Device Description

Ambu Neuroline Inoject Kit

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
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IKT Electrode, needle, diagnostic electromyograph

GMDN Terms

Code Name
11441 Electromyographic needle electrode, single-use

Identifiers

Type ID
Primary 05707480105861

Customer Contacts

Phone
+14107686464

Device Sizes

Type Value Unit Text
Length 35 Millimeter
Length 25 Millimeter
Length 38 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
10 – 40 Degrees Celsius