FDA UDI In Commercial Distribution 🇺🇸 United States

TendoNova Ocelot

DI: 00860009899872 · Model: DU1F30L-K · Tendonova Corporation
Product Codes
1
GMDN Terms
5
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TendoNova Ocelot
Primary DI
00860009899872
Version / Model
DU1F30L-K
Company Name
Tendonova Corporation
Labeler DUNS
115587907
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-07
Public Version
1
Public Version Date
2023-12-15
Public Version Status
New
Public Device Record Key
f667067a-8601-4391-bc6a-7d977fd7ba51

Device Description

TendoNova Disposable Unit 30mm Kit-Single

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
LFL Instrument, ultrasonic surgical

GMDN Terms

Code Name
44990 Skin-cover adhesive strip, non-antimicrobial
47787 Ophthalmic surgical instrument handle, pneumatic
47783 Patient surgical drape, single-use
15321 Skin topical coupling gel
44755 Soft-tissue ultrasonic surgical system handpiece tip, single-use

Identifiers

Type ID
Primary 00860009899872

Premarket Submissions

Submission Number Supplement Number
K212049 000

Device Sizes

Type Value Unit Text
Length 30 Millimeter