FDA UDI In Commercial Distribution 🇺🇸 United States

Precept®

DI: 10814707021032 · Model: 5200 · PRECEPT MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
125

Basic Information

Brand Name
Precept®
Primary DI
10814707021032
Version / Model
5200
Company Name
PRECEPT MEDICAL PRODUCTS, INC.
Labeler DUNS
783912892
Distribution Status
In Commercial Distribution
Device Count in Pkg
125
Record Status
Published
Publish Date
2018-09-18
Public Version
2
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
9a765944-0bfa-419d-847d-f323f1d78733

Device Description

Standard Surgeon's Caps

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
No

Product Codes

Code Name
FYF Cap, Surgical

GMDN Terms

Code Name
32297 Surgical cap, single-use

Identifiers

Type ID
Package 20814707021039
Primary 10814707021032
Unit of Use 00814707021035

Customer Contacts

Phone
800-438-5827