FDA UDI In Commercial Distribution 🇺🇸 United States

Precept®

DI: 10814707023371 · Model: 50096 · PRECEPT MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Precept®
Primary DI
10814707023371
Version / Model
50096
Company Name
PRECEPT MEDICAL PRODUCTS, INC.
Labeler DUNS
783912892
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-09-03
Public Version
1
Public Version Date
2020-09-11
Public Version Status
New
Public Device Record Key
110bfe0b-6c53-42d4-9de8-ca813701eba0

Device Description

Isolation Gown with Elastic Cuffs - AAMI 2

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
OEA Non-Surgical Isolation Gown

GMDN Terms

Code Name
35492 Isolation gown, single-use

Identifiers

Type ID
Package 20814707023378
Primary 10814707023371
Unit of Use 00814707023374

Customer Contacts

Phone
800-438-5827