FDA UDI In Commercial Distribution 🇺🇸 United States

PROFEMUR TL2

DI: 00192629396180 · Model: PRTL2BP8 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
PROFEMUR TL2
Primary DI
00192629396180
Version / Model
PRTL2BP8
Catalog Number
PRTL2BP8
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-13
Public Version
1
Public Version Date
2024-03-21
Public Version Status
New
Public Device Record Key
7ab7d210-5dc6-4528-97c5-6dbd365e63b7

Device Description

PROFEMUR TL2 BROACH SZ 8+

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
HWT TEMPLATE

GMDN Terms

Code Name
58481 Femoral stem prosthesis trial

Identifiers

Type ID
Secondary M684PRTL2BP81
Primary 00192629396180

Customer Contacts