FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964569463 · Model: MD217R · 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
04046964569463
Version / Model
MD217R
Catalog Number
MD217R
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-08
Public Version
1
Public Version Date
2020-05-18
Public Version Status
New
Public Device Record Key
35f0d4a4-9421-4e9b-b28e-4f222f00b669

Device Description

CERVICAL CUR 00000 STR 253MM SILVER

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
FZS CURETTE, SURGICAL, GENERAL USE

GMDN Terms

Code Name
32594 Intrauterine curette, manual

Identifiers

Type ID
Primary 04046964569463

Customer Contacts