FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964574269 · Model: MN008R · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046964574269
Version / Model
MN008R
Catalog Number
MN008R
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-06
Public Version
1
Public Version Date
2020-05-14
Public Version Status
New
Public Device Record Key
fa2f0cdd-c1df-4852-a16b-66833343c7ba

Device Description

, 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
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
GEG ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
11290 Open-surgery dissector

Identifiers

Type ID
Primary 04046964574269

Customer Contacts