FDA UDI In Commercial Distribution 🇺🇸 United States

ELMED

DI: 00842180184916 · Model: 32-12-12A · ELMED INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ELMED
Primary DI
00842180184916
Version / Model
32-12-12A
Catalog Number
32-12-12A
Company Name
ELMED INCORPORATED
Labeler DUNS
049290364
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-18
Public Version
1
Public Version Date
2024-01-26
Public Version Status
New
Public Device Record Key
4c26edb1-01dd-4fc8-adea-91a75ded9365

Device Description

WEISEMAN PEDERSON VAGINAL SPECULUM , 45 DEG HANDLE, RIGHT SIDE OPEN, MEDIUM BLADE SIZE 4" X 7/8"

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
Yes
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 00842180184916

Customer Contacts

Phone
224-353-6446