FDA UDI In Commercial Distribution 🇺🇸 United States

TEKNA Manufacturing Pvt. Ltd.

DI: 08906124940005 · Model: Modular Rectangular 6000 + 0 0 8 2 D/L · TEKNA MANUFACTURING PRIVATE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TEKNA Manufacturing Pvt. Ltd.
Primary DI
08906124940005
Version / Model
Modular Rectangular 6000 + 0 0 8 2 D/L
Company Name
TEKNA MANUFACTURING PRIVATE LIMITED
Labeler DUNS
876896922
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-29
Public Version
1
Public Version Date
2023-10-09
Public Version Status
New
Public Device Record Key
db12a3b8-619e-4d93-9e9c-909ce7e20a20

Device Description

Modular Multiplace hyperbaric chamber consisting of ASME 'U' stamped pressure vessel that can accommodate 8 patients in the main lock and 2 patients in the entry lock and a control console for the same. The entire system is ASME PVHO-1 compliant.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CBF Chamber, Hyperbaric

GMDN Terms

Code Name
12061 Hyperbaric chamber, stationary

Identifiers

Type ID
Primary 08906124940005

Customer Contacts

Phone
999-999-9999

Premarket Submissions

Submission Number Supplement Number
K002794 000