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ZLB - BBP/FA - Bonneville Power - Personal Protection - Refill

FDA UDI

Class II (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name
ZLB - BBP/FA - Bonneville Power - Personal Protection - Refill FDA UDI
Generic Name
Dressing-fixation skin adhesive tape, non-silicone FDA UDI
Device Name
ZLB - BBP/FA - Bonneville Power - Personal Protection - Refill FDA UDI
Model / Reference
FKR207-002 FDA UDI
Description
ZLB - BBP/FA - Bonneville Power - Personal Protection - Refill FDA UDI

Identifiers

Catalog Number
FKR207-002 FDA UDI
Primary DI / UDI-DI
00766588070025 FDA UDI
FDA Product Code
CBP FDA UDI
LRR FDA UDI
EFQ FDA UDI
KGX FDA UDI
GMDN Term
Dressing-fixation skin adhesive tape, non-silicone FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5870 FDA UDI
880.5240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: First aid kit, medicatedWound-nonadherent dressing, absorbent, non-antimicrobialDressing-fixation skin adhesive tape, non-siliconeNon-rebreathing valve, single-use

ZLB - BBP/FA - Bonneville Power - Personal Protection - Refill by Certified Safety Manufacturing, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Cardiopulmonary resuscitation mask, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 29c174a6-c6f6-44dd-8c21-5312fe1b4d86 35 fields · synced Jun 8, 2026