FDA UDI In Commercial Distribution 🇺🇸 United States

Precept®

DI: 00814707020700 · Model: 6601 · PRECEPT MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Precept®
Primary DI
00814707020700
Version / Model
6601
Company Name
PRECEPT MEDICAL PRODUCTS, INC.
Labeler DUNS
783912892
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-18
Public Version
1
Public Version Date
2018-10-19
Public Version Status
New
Public Device Record Key
7b7429e9-cea6-4880-b872-4d7d9d4e1bd2

Device Description

Patient Welcome Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
LRO General Surgery Tray

GMDN Terms

Code Name
61938 Surgical/examination garment kit

Identifiers

Type ID
Primary 00814707020700
Package 20814707020704

Customer Contacts

Phone
800-438-5827