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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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BodySupply Grip Wrap — 4 UDI-DI variants, MDR

MD Atlas
PROFESSIONAL BODY SUPPLY S.R.L. UNIPERSONALE

Data from EUDAMED, last updated May 31, 2026

BodySupply Grip Wrap

805540038PBSCOBA9

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: PROFESSIONAL BODY SUPPLY S.R.L. UNIPERSONALE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805540038PBSCOBA9
Device name: BodySupply Grip Wrap
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 2, 2026

Manufacturer & authorised representative

Manufacturer

Name: PROFESSIONAL BODY SUPPLY S.R.L. UNIPERSONALE
SRN: IT-MF-000028543
Country: Italy
Email: michele@bodysupply.com
Phone: +390854460528

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KJQ5B37DG20Z9J60GKJ865ME

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

PBSCOB50-PI/1208055400380315
PBSCOB25-PI/2408055400380292
PBSCOB25-BK/2408055400380285
PBSCOB50-BK/1208055400380308