FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653019922 · Model: BB512 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
AESCULAP
Primary DI
04038653019922
Version / Model
BB512
Catalog Number
BB512
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-04-17
Public Version
3
Public Version Date
2021-01-22
Public Version Status
Update
Public Device Record Key
d2b2c318-b826-4419-8d27-4ca56c87cb1e

Device Description

Scalpel Blades, Fig. 12, carbon steel, sterile, disposable, dispenser packaging, package of 100 pieces

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GES BLADE, SCALPEL

GMDN Terms

Code Name
37445 Manual scalpel blade, single-use

Identifiers

Type ID
Unit of Use 04038653338405
Primary 04038653019922

Customer Contacts