FDA UDI In Commercial Distribution 🇺🇸 United States

Tenoglide®

DI: 10381780032458 · Model: TG451 · Integra Lifesciences Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Tenoglide®
Primary DI
10381780032458
Version / Model
TG451
Catalog Number
TG451
Company Name
Integra Lifesciences Corporation
Labeler DUNS
083171244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-23
Public Version
7
Public Version Date
2023-05-16
Public Version Status
Update
Public Device Record Key
23996b1d-27a0-41c9-8ecc-646ef0edc3c9

Device Description

TenoGlide tendon protector sheet 4 in x 5 in (10cm x 12.5cm)

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
FTM Mesh, surgical

GMDN Terms

Code Name
35671 Tendon spacer

Identifiers

Type ID
Secondary M269TG4511
Primary 10381780032458

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K053655 000

Device Sizes

Type Value Unit Text
Width 10 Centimeter
Length 12.5 Centimeter
Width 4 Inch
Length 5 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store Flat
Type
Handling Environment Temperature
Temperature Range
2 – 30 Degrees Celsius