Identity
- Trade Name
- BCG Vaccine (Multiple Puncture Device) FDA UDI
- Generic Name
- Allergy testing lancet FDA UDI
- Model / Reference
- 1039922 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00300858999991 FDA UDI
- FDA Product Code
- LDH FDA UDI
- GMDN Term
- Allergy testing lancet FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Radiation Sterilization FDA UDI
Category: Allergy testing lancet
BCG Vaccine (Multiple Puncture Device) by Merck, Sharp & Dohme — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Merck, Sharp & Dohme
Sources (1)
- FDA UDI d3018e01-0d77-45ff-a104-62f9f212d6e9 33 fields · synced May 30, 2026