FDA UDI Not in Commercial Distribution 🇺🇸 United States

Biolon

DI: 00369918000008 · Model: version 1 · AMRING PHARMACEUTICALS INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Biolon
Primary DI
00369918000008
Version / Model
version 1
Catalog Number
62501
Company Name
AMRING PHARMACEUTICALS INC.
Labeler DUNS
079843051
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-17
Public Version
5
Public Version Date
2023-11-27
Public Version Status
Update
Public Device Record Key
2749f09b-5e7c-439c-986a-e3a4ed6a8fed
Distribution End Date
2020-09-15

Device Description

Viscoelastic surgical aid

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
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
LZP AID, SURGICAL, VISCOELASTIC

GMDN Terms

Code Name
35907 Vitreous/aqueous humour replacement medium, intraoperative

Identifiers

Type ID
Package 01369918000007
Primary 00369918000008

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 ml of Biolon solution in prefilled syringe
Total Volume 1 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not Freeze
Type
Special Storage Condition, Specify
Special Conditions
Protect from light
Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius