FDA UDI Not in Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964910340 · Model: US106 · AESCULAP, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046964910340
Version / Model
US106
Catalog Number
US106
Company Name
AESCULAP, INC.
Labeler DUNS
082594540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2023-09-06
Public Version Status
Update
Public Device Record Key
5abc9362-a9b5-4503-a802-0719915da795
Distribution End Date
2023-07-01

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
GCX APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED

GMDN Terms

Code Name
38749 Surgical/emergency suction cannula, non-illuminating, reusable

Identifiers

Type ID
Primary 04046964910340

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP AWAY FROM HEAT SOURCE
Type
Special Storage Condition, Specify