FDA UDI Not in Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653037414 · Model: DO612R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653037414
Version / Model
DO612R
Catalog Number
DO612R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-17
Public Version
3
Public Version Date
2021-10-28
Public Version Status
Update
Public Device Record Key
6cf31b03-a811-4c54-9ba2-f792812f3760
Distribution End Date
2021-04-22

Device Description

PARTSCH Raspatory, curved, 6", (150 mm), spoon shaped, sharp, #2, width: 4,600 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
EMJ ELEVATOR, SURGICAL, DENTAL

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 04038653037414

Customer Contacts