← Back to catalogue

Glide

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 91000-GL-FModel Glide - For Motion Control Standard Wrist or Ottobock 10S17 Wrist Configuration

by Infinite Biomedical Technologies LLC

Identity

Trade Name
Glide EUDAMEDFDA UDI
Generic Name
Myoelectric hand prosthesis FDA UDI
Device Name
Glide EUDAMED
For Steeper Espire Pro/Hybrid elbow configurations FDA UDI
Model / Reference
Glide - For Motion Control Standard Wrist or Ottobock 10S17 Wrist Configuration EUDAMED
91000-GL-F EUDAMEDFDA UDI
Description
For Steeper Espire Pro/Hybrid elbow configurations FDA UDI

Identifiers

Primary DI / UDI-DI
00850004850664 EUDAMEDFDA UDI
Basic UDI-DI
850004850GLIDE4C EUDAMED
510(k) Number
K240884 FDA UDI
FDA Product Code
IQZ FDA UDI
GXY FDA UDI
EMDN Code
Y240918 CONTROL SENSORS EUDAMED
GMDN Term
Myoelectric hand prosthesis FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.3420 FDA UDI
882.1320 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Glide by Infinite Biomedical Technologies LLC — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000007619
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (2)

  • EUDAMED d3b78943-a91d-43b7-8965-7a35bff41c12 61 fields · synced Jul 18, 2026
  • FDA UDI f5a665da-04aa-48a3-a081-6f3c3cbe66e5 34 fields · synced May 30, 2026