Identity
- Trade Name
- ZLB - UP8 UPRR - Locomotive - Refill FDA UDI
- Generic Name
- Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
- Device Name
- ZLB - UP8 UPRR - Locomotive - Refill FDA UDI
- Model / Reference
- KR619-627 FDA UDI
- Description
- ZLB - UP8 UPRR - Locomotive - Refill FDA UDI
Identifiers
- Catalog Number
- KR619-627 FDA UDI
- Primary DI / UDI-DI
- 00766588199276 FDA UDI
- FDA Product Code
- EFQ FDA UDILRR FDA UDIKGX FDA UDICBP FDA UDI
- GMDN Term
- Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Classification
- Device Class
- U FDA UDI
- Regulation Number
- 880.5240 FDA UDI868.5870 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, medicatedAdhesive bandageNon-woven gauze padWound-nonadherent dressing, absorbent, non-antimicrobial
ZLB - UP8 UPRR - Locomotive - Refill by Certified Safety Manufacturing, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class U | Pending data |
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Manufacturer
- Manufacturer
- Certified Safety Manufacturing, Inc.
Sources (1)
- FDA UDI f49e4e7f-73c7-426f-87a9-d238ba8d8bd3 35 fields · synced May 30, 2026