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Electric Wheeled Stretcher Standard, Flat Narrow Mattress, English

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 20582-021

by Sechrist Industries Inc

Identity

Trade Name
Sechrist Industries, Inc. FDA UDI
Generic Name
Hospital stretcher, manual FDA UDI
Device Name
Electric Wheeled Stretcher Standard, Flat Narrow Mattress, English EUDAMED
ELECTR. WHLD. STRCHR. STD. FLAT. NARROW MATTRESS, ENGLISH FDA UDI
Model / Reference
20582-021 EUDAMEDFDA UDI
Description
ELECTR. WHLD. STRCHR. STD. FLAT. NARROW MATTRESS, ENGLISH FDA UDI

Identifiers

Primary DI / UDI-DI
00850073470015 EUDAMEDFDA UDI
Basic UDI-DI
B-00850073470015 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 Standard, Flat Narrow Mattress, English by Sechrist Industries Inc — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID

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 2d0bd460-e169-447d-b1ce-451696933dee 61 fields · synced Jun 19, 2026
  • FDA UDI 0c2b3900-2145-4806-aa34-7f84f61a0cbe 35 fields · synced May 30, 2026