FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046963365578 · Model: MD569 · 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
04046963365578
Version / Model
MD569
Catalog Number
MD569
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-08
Public Version
1
Public Version Date
2020-07-16
Public Version Status
New
Public Device Record Key
005f2584-445a-40d5-a2e5-317d1fae3e17

Device Description

Dissecting Forceps, angled, 90 °, 5 1/2", (140 mm), 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
HTD FORCEPS

GMDN Terms

Code Name
62468 Surgical soft-tissue manipulation forceps, scissors-like, reusable

Identifiers

Type ID
Primary 04046963365578

Customer Contacts