FDA UDI In Commercial Distribution 🇺🇸 United States

INTREPID®

DI: 00380657528851 · Model: 8065752885 · Alcon Laboratories, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
INTREPID®
Primary DI
00380657528851
Version / Model
8065752885
Company Name
Alcon Laboratories, Inc.
Labeler DUNS
008018525
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-31
Public Version
1
Public Version Date
2020-09-08
Public Version Status
New
Public Device Record Key
706e8139-be4c-4191-a447-0ad7999247b2

Device Description

INTREPID® Transformer IA HP

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HMX Cannula, ophthalmic

GMDN Terms

Code Name
46705 Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

Identifiers

Type ID
Package 10380657528858
Primary 00380657528851

Customer Contacts