FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964572159 · Model: MF390T · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
AESCULAP
Primary DI
04046964572159
Version / Model
MF390T
Catalog Number
MF390T
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-30
Public Version
1
Public Version Date
2019-05-08
Public Version Status
New
Public Device Record Key
82cf1e2a-3419-466a-92e3-4a4c0c49b9dd

Device Description

Retractor Blade, toothed, opening width: 60 mm, titanium, non-sterile, reusable

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
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
GZT RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY

GMDN Terms

Code Name
45918 Hand-held surgical retractor, reusable

Identifiers

Type ID
Primary 04046964572159

Customer Contacts