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Electric Wheeled Stretcher EZ LOAD without Stretcher Plate, without mattress, E…

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 20582-S-231

by Sechrist Industries Inc

Identity

Trade Name
Sechrist Industries, Inc. FDA UDI
Generic Name
Hospital stretcher, manual FDA UDI
Device Name
Electric Wheeled Stretcher EZ LOAD without Stretcher Plate, without mattress, English EUDAMED
ELECTR. WHLD. STRCHR EZ LOAD. W/OUT STRCHR PLT, W/OUT MATTR, ENGLISH FDA UDI
Model / Reference
20582-S-231 EUDAMEDFDA UDI
Description
ELECTR. WHLD. STRCHR EZ LOAD. W/OUT STRCHR PLT, W/OUT MATTR, ENGLISH FDA UDI

Identifiers

Primary DI / UDI-DI
00850073470039 EUDAMEDFDA UDI
Basic UDI-DI
B-00850073470039 EUDAMED
FDA Product Code
FPO FDA UDI
EMDN Code
V08050199 PATIENT TRANSFER STRETCHERS - OTHER EUDAMED
GMDN Term
Hospital stretcher, manual FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.6910 FDA UDI
Market of Registration
Lithuania 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Depth — 91 Inch FDA UDI
Weight — 400 Pound FDA UDI
Height — 18 Inch FDA UDI
Width — 33.5 Inch FDA UDI

Electric Wheeled Stretcher EZ LOAD without Stretcher Plate, without mattress, E… by Sechrist Industries Inc — Class I — MDD, FDA UDI — listed in EUDAMED, FDA…

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000017869
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 56e42260-699b-4ef6-aad4-44a147497845 61 fields · synced Jun 18, 2026
  • FDA UDI 43ba3925-54de-421b-b95a-25d82e04cd8c 35 fields · synced May 30, 2026