FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653013791 · Model: OP290R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653013791
Version / Model
OP290R
Catalog Number
OP290R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-17
Public Version
1
Public Version Date
2020-04-27
Public Version Status
New
Public Device Record Key
9a37786c-a57c-43fb-867b-071f04ac5265

Device Description

Chest Support, for adults, for children, 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
LRC INSTRUMENT, ENT MANUAL SURGICAL

GMDN Terms

Code Name
35967 Surgical retraction system mounting frame, reusable

Identifiers

Type ID
Primary 04038653013791

Customer Contacts