FDA UDI In Commercial Distribution 🇺🇸 United States

Millennium

DI: 00190776199883 · Model: 91-92017 · Avalign Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Millennium
Primary DI
00190776199883
Version / Model
91-92017
Company Name
Avalign Technologies, Inc.
Labeler DUNS
792528510
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-02
Public Version
2
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
71f2ce82-1028-4abf-aaca-f4f14f59ae57

Device Description

LLETZ PEDERSON SPECULUM EVACUATION TUBE

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
Yes
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
HDF SPECULUM, VAGINAL, METAL

GMDN Terms

Code Name
35352 Vaginal speculum, reusable

Identifiers

Type ID
Primary 00190776199883

Customer Contacts