FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964685644 · Model: MA822T · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046964685644
Version / Model
MA822T
Catalog Number
MA822T
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-25
Public Version
1
Public Version Date
2020-09-02
Public Version Status
New
Public Device Record Key
9f4fb635-697b-4965-9c12-a53ee179de2b

Device Description

LESTER IOL MANIPULTR ANG .2MM DIA 115MM

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
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
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
HNQ Hook, ophthalmic

GMDN Terms

Code Name
33542 Bone hook

Identifiers

Type ID
Primary 04046964685644

Customer Contacts