FDA UDI In Commercial Distribution 🇺🇸 United States

Trel-X Putty

DI: 10381780112488 · Model: TXP10 · Integra Lifesciences Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Trel-X Putty
Primary DI
10381780112488
Version / Model
TXP10
Catalog Number
TXP10
Company Name
Integra Lifesciences Corporation
Labeler DUNS
083171244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-22
Public Version
5
Public Version Date
2020-09-22
Public Version Status
Update
Public Device Record Key
3112385b-0b1e-4627-840c-f1c768325740

Device Description

Trel-X™Putty, 10cc is human bone that has been demineralized and combined with poloxamer reverse phase medium which is formulated into a gel or putty-like form. Trel-X is provided in a sterile, single patient use package.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
Yes
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
MQV FILLER, BONE VOID, CALCIUM COMPOUND

GMDN Terms

Code Name
47257 Bone matrix implant, human-derived

Identifiers

Type ID
Secondary M386TXP101
Primary 10381780112488

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K040419 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 10cc

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
15 – 30 Degrees Celsius