FDA UDI In Commercial Distribution 🇺🇸 United States

VOLMED BRASIL

DI: 07908783000367 · Model: AAGU03 - S.O · VOLMED BRASIL EQUIPAMENTOS LTDA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
VOLMED BRASIL
Primary DI
07908783000367
Version / Model
AAGU03 - S.O
Company Name
VOLMED BRASIL EQUIPAMENTOS LTDA
Labeler DUNS
903156736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-06
Public Version
1
Public Version Date
2025-03-14
Public Version Status
New
Public Device Record Key
00ed215c-724f-4a50-8796-7ed2fa332fda

Device Description

VOLMED SCORPION II SUTURE NEEDLE

Device Characteristics

Single Use
Yes
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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GAB Needle, Suturing, Disposable

GMDN Terms

Code Name
61143 Suturing needle, single-use

Identifiers

Type ID
Primary 07908783000367