FDA UDI In Commercial Distribution 🇺🇸 United States

Laparoscope

DI: 06973031299603 · Model: 20533FA · Guangdong Optomedic Technologies, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Laparoscope
Primary DI
06973031299603
Version / Model
20533FA
Company Name
Guangdong Optomedic Technologies, Inc.
Labeler DUNS
544527790
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-26
Public Version
1
Public Version Date
2024-04-03
Public Version Status
New
Public Device Record Key
0fd5a173-2897-4f2a-b5c6-0c6fc2491ebc

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization, Hydrogen Peroxide

Product Codes

Code Name
GCJ Laparoscope, General & Plastic Surgery
HET Laparoscope, Gynecologic (And Accessories)
NMH Laparoscope And Accessories, Gynecologic, Reprocessed

GMDN Terms

Code Name
12291 Rigid optical laparoscope

Identifiers

Type ID
Primary 06973031299603

Premarket Submissions

Submission Number Supplement Number
K231003 000