Identity
- Trade Name
- ZLB - 10 - Metra 49-980170 FDA UDI
- Generic Name
- First aid kit, medicated FDA UDI
- Device Name
- ZLB - 10 - Metra 49-980170 FDA UDI
- Model / Reference
- K608-016 FDA UDI
- Description
- ZLB - 10 - Metra 49-980170 FDA UDI
Identifiers
- Catalog Number
- K608-016 FDA UDI
- Primary DI / UDI-DI
- 00766588080161 FDA UDI
- FDA Product Code
- CBP FDA UDILRR FDA UDIEFQ FDA UDIKGX FDA UDI
- GMDN Term
- First aid kit, medicated FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5870 FDA UDI880.5240 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, medicatedAdhesive bandageNon-woven gauze padWound-nonadherent dressing, absorbent, non-antimicrobial
ZLB - 10 - Metra 49-980170 by Certified Safety Manufacturing, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Emergency Rescue Mask — CBX LLC · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Certified Safety Manufacturing, Inc.
Sources (1)
- FDA UDI dcc59e62-1f7f-4769-b395-a26512700383 35 fields · synced Jun 8, 2026