FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653151202 · Model: EA993 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
AESCULAP
Primary DI
04038653151202
Version / Model
EA993
Catalog Number
EA993
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
e3dad57e-2bde-4f53-89c4-3e1a14d44a79

Device Description

LIGATURE RUBBER RINGS

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FHN Ligator, hemorrhoidal

GMDN Terms

Code Name
36176 Polypectomy endoscopic ligator, reusable

Identifiers

Type ID
Primary 04038653151202
Unit of Use 04038653340880

Customer Contacts