FDA UDI In Commercial Distribution 🇺🇸 United States

Avalign

DI: 00190776006709 · Model: VM57-3941 · Avalign Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Avalign
Primary DI
00190776006709
Version / Model
VM57-3941
Company Name
Avalign Technologies, Inc.
Labeler DUNS
792528510
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-23
Public Version
4
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
24e6d0f8-0b1a-4f07-b82b-e514c1d09744

Device Description

Heany Clamp curved horizontal serrated

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
No
Has Lot/Batch Number
Yes
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
HCZ FORCEPS, SURGICAL, GYNECOLOGICAL

GMDN Terms

Code Name
11775 Open-surgery biopsy forceps, reusable

Identifiers

Type ID
Primary 00190776006709

Customer Contacts

Device Sizes

Type Value Unit Text
Length 12 Inch