FDA UDI In Commercial Distribution 🇺🇸 United States

ULTRA FLOW

DI: 00380657517954 · Model: 8065751795 · Alcon Laboratories, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ULTRA FLOW
Primary DI
00380657517954
Version / Model
8065751795
Company Name
Alcon Laboratories, Inc.
Labeler DUNS
008018525
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-07
Public Version
6
Public Version Date
2019-10-07
Public Version Status
Update
Public Device Record Key
7b3321ed-ec03-4b3b-b59a-ab0c2ef5574d

Device Description

ULTRAFLOW II I/A HANDPIECE

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NKK NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED

GMDN Terms

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

Identifiers

Type ID
Primary 00380657517954

Customer Contacts