FDA UDI In Commercial Distribution 🇺🇸 United States

Withdrawal Device

DI: 00817434020104 · Model: 502 · BRYMILL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Withdrawal Device
Primary DI
00817434020104
Version / Model
502
Catalog Number
502
Company Name
BRYMILL CORPORATION
Labeler DUNS
041116500
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-14
Public Version
4
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
47cea100-03e4-4c9e-97ed-3ed3582ef55a

Device Description

Hand Held Liquid Nitrogen Delivery System Accessory - Liquid Nitrogen Withdrawal Device

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
GEH Unit, Cryosurgical, Accessories

GMDN Terms

Code Name
11067 General cryosurgical system, cryogen gas, mechanical

Identifiers

Type ID
Primary 00817434020104