← Back to catalogue

BriteBlade Pro Single-Use Fiber Optic Wis-Hipple 1.5

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 040-00-1215U

by Flexicare Medical Limited

Identity

Trade Name
Flexicare EUDAMED
BriteBlade Pro Single-Use Fiber Optic Wis-Hipple 1.5 FDA UDI
Generic Name
Laryngoscope blade, single-use FDA UDI
Device Name
Single Use Laryngoscopes (Fibre Optic, Laryngoscope, Sterile) EUDAMED
Model / Reference
040-00-1215U EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05055788768708 EUDAMEDFDA UDI
Basic UDI-DI
B-05055788768708 EUDAMED
FDA Product Code
CCW FDA UDI
EMDN Code
R9002 LARYNGOSCOPE BLADES, SINGLE-USE EUDAMED
GMDN Term
Laryngoscope blade, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.5540 FDA UDI
Market of Registration
Northern Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

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

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laryngoscope blade, single-use

BriteBlade Pro Single-Use Fiber Optic Wis-Hipple 1.5 by Flexicare Medical Limited — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Laryngoscope blade, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI 0818bde3-d866-438b-83f6-bf7196ef0eef 32 fields · synced Oct 9, 2026
  • EUDAMED e5917be4-cf4a-453f-887c-1168adfa5701 61 fields · synced Oct 9, 2026