FDA UDI In Commercial Distribution 🇺🇸 United States

LYOPLANT

DI: 04038653700943 · Model: 1066021 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LYOPLANT
Primary DI
04038653700943
Version / Model
1066021
Catalog Number
1066021
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2022-03-14
Public Version Status
Update
Public Device Record Key
06b0a297-bd17-4793-b7e1-4a7f3407ac4c

Device Description

LYOPLANT 6X14CM

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
No
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
GXQ DURA SUBSTITUTE

GMDN Terms

Code Name
48155 Dura mater biomatrix implant

Identifiers

Type ID
Primary 04038653700943

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Width (mm) : 60.000 MM
Device Size Text, specify Length : 140.000 MM

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 30 Degrees Celsius