FDA UDI In Commercial Distribution 🇺🇸 United States

Surgical Direct

DI: B382SD4974P0 · Model: SD4974P · Surgical Direct, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Surgical Direct
Primary DI
B382SD4974P0
Version / Model
SD4974P
Catalog Number
SD4974P
Company Name
Surgical Direct, Inc.
Labeler DUNS
124367223
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-10
Public Version
1
Public Version Date
2023-04-18
Public Version Status
New
Public Device Record Key
e2e8dab8-e64f-4fd3-bb4d-61960b346d55

Device Description

Atraumatic Universal Extraction Forcep, Adult/ Pediatric/ Child F1P Upper Universal

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Manufacturing Date
No
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
EIX PROBE, PERIODONTIC

GMDN Terms

Code Name
15713 Dental rongeur

Identifiers

Type ID
Primary B382SD4974P0

Customer Contacts