FDA UDI In Commercial Distribution 🇺🇸 United States

Ahmed™ ClearPath

DI: 00892064002348 · Model: 250 · NEW WORLD MEDICAL, INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ahmed™ ClearPath
Primary DI
00892064002348
Version / Model
250
Catalog Number
CP250
Company Name
NEW WORLD MEDICAL, INCORPORATED
Labeler DUNS
622768711
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-23
Public Version
4
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
2c42358b-376b-4a1b-8887-b49481576722

Device Description

Silicone Valveless Glaucoma Drainage Device

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
MR Safe
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KYF IMPLANT, EYE VALVE

GMDN Terms

Code Name
61127 Glaucoma shunt

Identifiers

Type ID
Primary 00892064002348

Customer Contacts

Device Sizes

Type Value Unit Text
Area/Surface Area 250 Square millimeter