FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: B58208017840 · Model: 0801784 · GEORGE TIEMANN & CO.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
B58208017840
Version / Model
0801784
Catalog Number
0801784
Company Name
GEORGE TIEMANN & CO.
Labeler DUNS
107043630
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
1
Public Version Date
2020-10-02
Public Version Status
New
Public Device Record Key
92ea2e18-f83b-410f-bcc0-cabea870bfe4

Device Description

RETRACTOR, ALL TYPES

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EIG RETRACTOR, ALL TYPES

GMDN Terms

Code Name
45918 Hand-held surgical retractor, reusable

Identifiers

Type ID
Primary B58208017840

Customer Contacts

Phone
+1(631)273-0005 ext. 5223