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Blast® Modular Bandage

EUDAMEDFDA UDI

Class I (EU MDR)

Ref BLAST

by TacMed Solutions, LLC

Identity

Trade Name
BLAST® MODULAR BANDAGE EUDAMED
Blast Bandage FDA UDI
Generic Name
First aid absorbent pad/bandage FDA UDI
Device Name
BLAST® MODULAR BANDAGE EUDAMED
The BLAST® Bandage was designed to provide the ability to quickly package traumatic amputations, burns, and large pattern wounds with minimal use of supplies and minimal effort. The BLAST® Bandage provides a 20" X 20" treatment area, but packs to about the size of a 4” combat bandage. Our large non-adherent wound pad can be easily wrapped around limbs and secured with the attached elastic wrap. It provides a large sterile protective covering for shrapnel wounds or burns. With such a large coverage area, the Blast® Bandage is large enough to cover the entire back or chest of most casualties. The BLAST® Bandage also offers a removable occlusive layer that will cover a 19"x 19" area or can be used to cover abdominal contents minimizing the loss of heat and moisture. As with our other bandages, the "brakes" on the bandage help prevent accidental unrolling of the elastic wrap during high stress application. These brakes are especially helpful during the dressing of amputations. By providing multiple points of adhesion, the brakes prevent slippage of the elastic during the wrapping process. This creates a more secure, effective bandage and decreases the chance of the wound being exposed during movement. FDA UDI
Model / Reference
BLAST EUDAMED
A FDA UDI
Description
The BLAST® Bandage was designed to provide the ability to quickly package traumatic amputations, burns, and large pattern wounds with minimal use of supplies and minimal effort. The BLAST® Bandage provides a 20" X 20" treatment area, but packs to about the size of a 4” combat bandage. Our large non-adherent wound pad can be easily wrapped around limbs and secured with the attached elastic wrap. It provides a large sterile protective covering for shrapnel wounds or burns. With such a large coverage area, the Blast® Bandage is large enough to cover the entire back or chest of most casualties. The BLAST® Bandage also offers a removable occlusive layer that will cover a 19"x 19" area or can be used to cover abdominal contents minimizing the loss of heat and moisture. As with our other bandages, the "brakes" on the bandage help prevent accidental unrolling of the elastic wrap during high stress application. These brakes are especially helpful during the dressing of amputations. By providing multiple points of adhesion, the brakes prevent slippage of the elastic during the wrapping process. This creates a more secure, effective bandage and decreases the chance of the wound being exposed during movement. FDA UDI

Identifiers

Catalog Number
BLAST FDA UDI
Primary DI / UDI-DI
00818630010289 EUDAMEDFDA UDI
Basic UDI-DI
B-00818630010289 EUDAMED
FDA Product Code
MHW FDA UDI
EMDN Code
M0304010103 ELASTIC COMPRESSION BANDAGES, NON-ADHESIVE, HIGH EXTENSIBILITY (>140%) EUDAMED
GMDN Term
First aid absorbent pad/bandage FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.5075 FDA UDI
Market of Registration
Germany 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

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

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

Blast® Modular Bandage by TacMed Solutions, LLC — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000042757
Authorised Representative
Casus Europe B.V. NL-AR-000037688

Sources (2)

  • EUDAMED ba6ce3ae-49c1-4ad3-9b25-dcaea38a0eaf 61 fields · synced Jun 18, 2026
  • FDA UDI 21a3fc60-303f-4c78-abcb-2e8683cdb3bc 35 fields · synced May 30, 2026