FDA UDI In Commercial Distribution 🇺🇸 United States

Fenestrated Atraumatic Forceps Inner Shaft

DI: B354C2794 · Model: C279 · ORANGE SURGICAL INSTRUMENTS, LLC
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
60

Basic Information

Brand Name
Fenestrated Atraumatic Forceps Inner Shaft
Primary DI
B354C2794
Version / Model
C279
Company Name
ORANGE SURGICAL INSTRUMENTS, LLC
Labeler DUNS
047063695
Distribution Status
In Commercial Distribution
Device Count in Pkg
60
Record Status
Published
Publish Date
2023-07-14
Public Version
2
Public Version Date
2024-01-01
Public Version Status
Update
Public Device Record Key
9b3223e1-ca05-4030-bc1b-3553b4e7a727

Device Description

Fenestrated Atraumatic Forceps Inner Shaft

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Peracetic Acid

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
33596 Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
61875 Endoscopic electrosurgical electrode, monopolar, single-use

Identifiers

Type ID
Unit of Use B3542790
Primary B354C2794

Premarket Submissions

Submission Number Supplement Number
K101733 000