FDA UDI In Commercial Distribution 🇺🇸 United States

Precept®

DI: 10814707020882 · Model: 51178 · PRECEPT MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Precept®
Primary DI
10814707020882
Version / Model
51178
Company Name
PRECEPT MEDICAL PRODUCTS, INC.
Labeler DUNS
783912892
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
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
95928961-f4e0-49ee-a465-849cdc63c908

Device Description

Isolation Gown - AAMI Level 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 20814707020889
Primary 10814707020882
Unit of Use 00814707020885

Customer Contacts

Phone
800-438-5827