FDA UDI In Commercial Distribution 🇺🇸 United States

ROTEPS SHAFT

DI: 14063108105773 · Model: 02BRT20460 · NOVATECH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ROTEPS SHAFT
Primary DI
14063108105773
Version / Model
02BRT20460
Company Name
NOVATECH
Labeler DUNS
777211640
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-01
Public Version
1
Public Version Date
2024-10-09
Public Version Status
New
Public Device Record Key
f06fa50f-96b1-4ac1-8a85-95490b0ba118

Device Description

Shaft Ø 4 mm, L 60 cm

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
No
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
KAE Forceps, Ent

GMDN Terms

Code Name
35080 Rigid endoscopic tissue manipulation forceps, reusable

Identifiers

Type ID
Primary 14063108105773