FDA UDI In Commercial Distribution 🇺🇸 United States

Amnicot

DI: 09350902000174 · Model: Amnicot English · GO MEDICAL INDUSTRIES PTY. LTD.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Amnicot
Primary DI
09350902000174
Version / Model
Amnicot English
Catalog Number
ACD01-E
Company Name
GO MEDICAL INDUSTRIES PTY. LTD.
Labeler DUNS
757634266
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
50eafec5-2799-4281-baa8-55c499b33e04

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HGE Amniotome

GMDN Terms

Code Name
46520 Amniotic membrane perforator, single-use

Identifiers

Type ID
Package 9350902000204
Primary 09350902000174
Package 9350902000198
Package 9350902000181

Premarket Submissions

Submission Number Supplement Number
K850758 000