FDA UDI In Commercial Distribution 🇺🇸 United States

E.M Adams co, inc.

DI: 10840200300602 · Model: 114-239-1 · E.M. ADAMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
E.M Adams co, inc.
Primary DI
10840200300602
Version / Model
114-239-1
Company Name
E.M. ADAMS, INC.
Labeler DUNS
001403807
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-14
Public Version
1
Public Version Date
2021-05-24
Public Version Status
New
Public Device Record Key
1f0763d5-b37f-4ab9-aebc-0d9a18e680ba

Device Description

SUTURE REMOVAL

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
MCZ Suture Removal Kit

GMDN Terms

Code Name
13894 Suture removal kit

Identifiers

Type ID
Package 50840200300594
Primary 10840200300602

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K812132 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 6" X 3.75" X 5"